ChemicalBook > CAS DataBase List > OTAVA-BB 1129464

OTAVA-BB 1129464

Product Name
OTAVA-BB 1129464
CAS No.
90868-92-1
Chemical Name
OTAVA-BB 1129464
Synonyms
OTAVA-BB 1129464;a-Cyclopropyl-4-bromo-benzylamine;alpha-Cyclopropyl-4-broMo-benzylaMine;(4-BROMOPHENYL)(CYCLOPROPYL)METHANAMINE;4-Bromo-α-cyclopropylbenzenemethanamine;Benzenemethanamine, 4-bromo-α-cyclopropyl-;1-(4-bromophenyl)-1-cyclopropylmethanamine;1-CYCLOPROPYL-1-(4-BROMOPHENYL)METHYLAMINE;Benzenemethanamine, 4-bromo-alpha-cyclopropyl-
CBNumber
CB72464021
Molecular Formula
C10H12BrN
Formula Weight
226.116
MOL File
90868-92-1.mol
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OTAVA-BB 1129464 Property

Boiling point:
305.7±17.0 °C(Predicted)
Density 
1.486±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
9.09±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety

HS Code 
2921490090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HCH0345631
Product name
(4-BROMOPHENYL)(CYCLOPROPYL)METHYLAMINE
Purity
95.00%
Packaging
0.25G
Price
$233
Updated
2021/12/16
AK Scientific
Product number
5132AC
Product name
(4-Bromophenyl)(cyclopropyl)methanamine
Packaging
250mg
Price
$471
Updated
2021/12/16
Apolloscientific
Product number
OR451108
Product name
a-Cyclopropyl-4-bromo-benzylamine
Packaging
1g
Price
$1158
Updated
2021/12/16
SynQuest Laboratories
Product number
3630-9-12
Product name
a-Cyclopropyl-4-bromobenzylamine
Packaging
1g
Price
$1277
Updated
2021/12/16
Ambeed
Product number
A319648
Product name
(4-Bromophenyl)(cyclopropyl)methanamine
Purity
95%
Packaging
1g
Price
$587
Updated
2021/12/16
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OTAVA-BB 1129464 Chemical Properties,Usage,Production

Synthesis

623-00-7

23719-80-4

90868-92-1

A solution of 4-bromobenzonitrile (6.30 g) in tetrahydrofuran (50 mL) was added dropwise to an ice-bath-cooled 0.5 M cyclopropylmagnesium bromide tetrahydrofuran solution (200 mL) over 20 minutes. The reaction mixture was stirred continuously for 5.5 hours under ice bath conditions. Subsequently, methanol (100 mL) was added slowly over 20 minutes to quench the reaction. After batchwise addition of sodium borohydride (2.65 g), the reaction mixture was gradually warmed to room temperature and stirred overnight. Upon completion of the reaction, saturated aqueous NaHCO3 was added and the pH of the mixture was adjusted to 8-9 with 1 M hydrochloric acid.The reaction mixture was extracted with dichloromethane and the organic phases were combined, washed with water and dried over anhydrous magnesium sulfate. The organic phase was concentrated under reduced pressure to give the crude product as an oil. The oil was redissolved in dichloromethane and extracted with 1 M hydrochloric acid. The combined aqueous phases were alkalized to pH 8-9 with 4M NaOH aqueous solution and extracted again with dichloromethane. The combined organic phases were washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give α-cyclopropyl-4-bromobenzylamine as an oily product. Yield: 5.56 g (72% yield); mass spectrum (ESI+): m/z = 209/211 (Br)[M+H-NH3]+.

References

[1] Patent: WO2010/139673, 2010, A1. Location in patent: Page/Page column 80; 81
[2] Patent: WO2017/156179, 2017, A1. Location in patent: Paragraph 00404; 00405; 00406

OTAVA-BB 1129464 Preparation Products And Raw materials

Raw materials

Preparation Products

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OTAVA-BB 1129464 Suppliers

Jia Xing Isenchem Co.,Ltd
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