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Cyclopropyl bromide

Product Name
Cyclopropyl bromide
CAS No.
4333-56-6
Chemical Name
Cyclopropyl bromide
Synonyms
BROMOCYCLOPROPANE;Cyclopropyl;BromocycL;NSC 89692;bromo-cyclopropan;1-Bromocyclopropane;CYCLOPROPYL BROMIDE;Cyclopropyl bromine;Cyclopropane, bromo-;Bromocyclopropane>
CBNumber
CB8421267
Molecular Formula
C3H5Br
Formula Weight
120.98
MOL File
4333-56-6.mol
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Cyclopropyl bromide Property

Boiling point:
69 °C (lit.)
Density 
1.51 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.458(lit.)
Flash point:
20 °F
storage temp. 
2-8°C
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Liquid
Specific Gravity
1.510
color 
Clear colorless
Water Solubility 
immiscible
BRN 
1900287
InChI
InChI=1S/C3H5Br/c4-3-1-2-3/h3H,1-2H2
InChIKey
LKXYJYDRLBPHRS-UHFFFAOYSA-N
SMILES
C1(Br)CC1
CAS DataBase Reference
4333-56-6(CAS DataBase Reference)
NIST Chemistry Reference
Cyclopropyl bromide(4333-56-6)
EPA Substance Registry System
Cyclopropane, bromo- (4333-56-6)
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Safety

Hazard Codes 
F,Xi
Risk Statements 
11-36/37/38
Safety Statements 
16-26-36-37/39
RIDADR 
UN 1993 3/PG 2
WGK Germany 
3
8-19
Hazard Note 
Irritant
TSCA 
T
HazardClass 
3
PackingGroup 
II
HS Code 
29035990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P243Take precautionary measures against static discharge.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C117307
Product name
Bromocyclopropane
Purity
99%
Packaging
5g
Price
$82.4
Updated
2025/07/31
Sigma-Aldrich
Product number
C117307
Product name
Bromocyclopropane
Purity
99%
Packaging
25g
Price
$175
Updated
2025/07/31
TCI Chemical
Product number
C1067
Product name
Bromocyclopropane
Purity
>98.0%(GC)
Packaging
5g
Price
$50
Updated
2025/07/31
TCI Chemical
Product number
C1067
Product name
Bromocyclopropane
Purity
>98.0%(GC)
Packaging
25g
Price
$145
Updated
2025/07/31
TCI Chemical
Product number
C1067
Product name
Bromocyclopropane
Purity
>98.0%(GC)
Packaging
250g
Price
$849
Updated
2025/07/31
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Cyclopropyl bromide Chemical Properties,Usage,Production

Description

Cyclopropyl bromide is also named as Bromocyclopropane. It is used in organic synthesis, for instance, for the formation of a Grignard Reagent, cyclopropyllithium. It is also used as an intermediate in the manufacture of pharmaceutical and agrochemical products.

Chemical Properties

Light yellow to clear colourless liquid, boiling point 67-69°C, refractive index (nD20) 1.4605, density (d420) 1.5120, flash point -6°C.

Uses

Bromocyclopropane is primarily used an intermediate in the manufacture of pharmaceutical and agrochemical products. It is also used in the production of cyclopropyl boric acid. It is used as an intermediate in organic synethesis.

Preparation

Bromocyclopropane has been prepared by the Hunsdiecker reaction by adding silver cyclopropanecarboxylate to bromine in dichlorodifluoromethane at ?29° (53% yield) or in tetrachloroethane at ?20° to ?25° (15–20% yield). Decomposition of the peroxide of cyclopropanecarboxylic acid in the presence of carbon tetrabromide gave bromocyclopropane in 43% yield. An attempt to prepare the bromide via the von Braun reaction was unsuccessful. Ten percent yields are reported for the photobromination of cyclopropane and the photochemical rearrangement of allyl bromide. Treatment of 1,1,3-tribromopropane with methyllithium prepared from methyl bromide furnishes a 60–65% yield of bromocyclopropane.

Application

Bromocyclopropane have anti-angiogenic effects that inhibits the growth of new blood vessels by interfering with the production of prostaglandins and nitric oxide, which are important for the formation of new blood vessels. Bromocyclopropane binds to cyclopropyl and hydrochloric acid, forming a hydrogen bond. It also forms a hydrogen bond with fatty acids and an a-type hydroxyl group.

Synthesis

1759-53-1

4333-56-6

(1) 179 g of 1,3-bromochloropropane was added to a three-necked flask, 29 g of potassium cyanide and 50 ml of water were added and heated and stirred until completely dissolved. Subsequently, 70 ml of ethanol solution was added and the mixture was stirred and refluxed for 2 hours. After completion of the reaction, it was cooled to room temperature and diluted with 300 ml of water to separate the oil and aqueous phases. The aqueous phase was extracted with 40 ml of chloroform, the organic phases were combined and dried with anhydrous calcium chloride. 316.9 g of hydrogen chloride was obtained. Chlorobutanenitrile 241.6 g was prepared by adding 100 ml of sodium hydroxide solution and stirring the reaction for 2 hours. Then 200 ml of water was added, cooled to about 10°C, 44 ml of concentrated sulfuric acid was added to acidify the reaction mixture, extracted with petroleum ether as an extractant, the organic phases were combined and dried with anhydrous sodium sulfate to obtain 330.1 g of cyclopropionic acid. (2) 324.8 g of cyclopropionic acid was added dropwise to a reaction flask with 48 g of mercuric oxide, 160 ml of a mixture of 1,1,2,2-tetrachloroethane and 64.4 g of liquid bromine, and stirred for 2 hours. After completion of the reaction, the mixture was cooled to 5°C, washed with tetrachloroethane and then dried with calcium chloride to give 419.15 g of bromocyclopropane.

References

Science of Synthesis: Houben-Weyl Methods of Molecular Transformation Vol. 7: Compounds of Group 13 and 2 (Al, Ga, In, Tl, Be…Ba), 2007, ISBN: 9783131484819
D. Seyferth, H. M. Cohen, The Stability of Cyclopropyllithium in diethyl ether and in tetrahydrofuran, Journal of Organometallic Chemistry, 1963, vol. 1, pp. 15-21
“Formal Nucleophilic Substitution of Bromocyclopropanes with Azoles”, Ryabchuk, P.; Rubina, M.; Xu, J.; Rubin, M. Org. Lett. 2012, 14, 1752.
“Formal Substitution of Bromocyclopropanes with Nitrogen Nucleophiles”, Banning, J. E.; Gentillon, J.; Ryabchuk, P. G.; Prosser, A. R.; Rogers, A.; Edwards, A.; Holtzen, A.; Babkov, I.; Rubina, M.; Rubin, M. J. Org. Chem., 2013, 78, 7601.

Cyclopropyl bromide Preparation Products And Raw materials

Raw materials

Preparation Products

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Cyclopropyl bromide Suppliers

goldenchemical
Tel
18651817751
Email
xisiyu@goldenchemical.com
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China
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1447
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Chem-Stone Co.,Ltd.
Tel
020-82185713,82185709 13418171485
Fax
020-82185696
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sales@chem-stone.com
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China
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Dalian Idery Biotechnology Co., Ltd.
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15141125520 15141125520
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0411-66160116
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3489496641@qq.com
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China
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Sichuan Weibo Science and Technology Co.,Ltd
Tel
028-65199188 13880582998
Fax
028-65199189
Email
ellnn@163.com
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China
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Aikon International Limited
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025-66061636 18013972705
Fax
(3)02557626880
Email
qqyang@aikonchem.com
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China
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15814
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Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
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025-66028182 18626450290
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yftan@aikonchem.com
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China
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Hefei QiChang Biological Technology Co., Ltd.
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18019964904; 17756579152
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QQ:252833506
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liuchun.0228@163.com
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China Haohua (Dalian) Research & Design Institute of Chemical Industry Co., Ltd
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13644955951
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0411-84678594
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623615430@qq.com
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China
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Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Fax
+86-21-57758967
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sales@boylechem.com
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China
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2208
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J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
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jkinfo@jkchemical.com
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China
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View Lastest Price from Cyclopropyl bromide manufacturers

R&D Scientific Inc.
Product
Bromocyclopropane 4333-56-6
Price
US $860.00/Kg
Min. Order
0.100Kg
Purity
99 %
Supply Ability
5000 Kg
Release date
2025-09-12
Henan Aochuang Chemical Co.,Ltd.
Product
Cyclopropyl bromide 4333-56-6
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-22
Sichuan Zhuoyu Yantang Technology Co., Ltd.
Product
Cyclopropyl bromide 4333-56-6
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2024-10-22

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