ChemicalBook > CAS DataBase List > 5-bromo-1-methyl-1H-indole-3-carboxylicacid

5-bromo-1-methyl-1H-indole-3-carboxylicacid

Product Name
5-bromo-1-methyl-1H-indole-3-carboxylicacid
CAS No.
400071-95-6
Chemical Name
5-bromo-1-methyl-1H-indole-3-carboxylicacid
Synonyms
5-Bromo-1-methylindole-3-carboxylic acid;5-bromo-1-methyl-1H-indole-3-carboxylicacid;1H-Indole-3-carboxylic acid, 5-bromo-1-methyl-
CBNumber
CB02484523
Molecular Formula
C10H8BrNO2
Formula Weight
254.08
MOL File
400071-95-6.mol
More
Less

5-bromo-1-methyl-1H-indole-3-carboxylicacid Property

Boiling point:
441.1±25.0 °C(Predicted)
Density 
1.65
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
Crystalline Powder
pka
3.80±0.30(Predicted)
color 
White to off-white
More
Less

Safety

HS Code 
29339980
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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

More
Less

N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FB144221
Product name
5-Bromo-1-methyl-1H-indole-3-carboxylic acid
Packaging
2g
Price
$300
Updated
2021/12/16
Activate Scientific
Product number
AS3795
Product name
5-Bromo-1-methyl-1H-indole-3-carboxylicacid
Purity
97+%
Packaging
5G
Price
$426
Updated
2021/12/16
ChemScene
Product number
CS-0028257
Product name
5-Bromo-1-methyl-1H-indole-3-carboxylicacid
Purity
99.23%
Packaging
10g
Price
$447
Updated
2021/12/16
ChemScene
Product number
CS-0028257
Product name
5-Bromo-1-methyl-1H-indole-3-carboxylicacid
Purity
99.23%
Packaging
1g
Price
$84
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB144221
Product name
5-Bromo-1-methyl-1H-indole-3-carboxylic acid
Packaging
250mg
Price
$85
Updated
2021/12/16
More
Less

5-bromo-1-methyl-1H-indole-3-carboxylicacid Chemical Properties,Usage,Production

Synthesis

10075-52-2

124-38-9

400071-95-6

In a 50 mL autoclave fitted with a glass inner tube and a magnetic stir bar, 5-bromo-1-methyl-1H-indole (1a, density 1.05 g/mL; 125 μL, 1.00 mmol), dimethylaluminum chloride (1.0 M hexane solution; 1.0 mL, 1.0 mmol), and toluene (1.0 mL) were added, and the mixture was purged with nitrogen under protection by repeated pressurization and subsequent swelling The final pressure was adjusted to 3.0 MPa using a carbon dioxide purge device.The mixture was stirred at 80 °C for 3 h before the reactor was allowed to cool to room temperature and slowly depressurized. The reaction mixture was quenched with 2 M hydrochloric acid solution and the aqueous layer was extracted with ethyl acetate. The combined organic layers were extracted with 0.5 M sodium carbonate solution and the extract was acidified by adding concentrated hydrochloric acid to release the free carboxylic acid and again extracted with ethyl acetate. The extract was dried with anhydrous magnesium sulfate and evaporated under reduced pressure to obtain the residue, which was purified by column chromatography using chloroform-ethyl acetate (1:1, v/v) as eluent to give 1-methyl-5-bromo-3-indolecarboxylic acid (2a) as crystals (168 mg, 96% yield). The carboxylation reaction of other indole derivatives was carried out in a similar way. The crude product was routinely purified by column chromatography using chloroform-ethyl acetate (1:1, v/v) or pure chloroform-ethyl acetate (1:1, v/v) containing 1% (v/v) acetic acid as eluent. The reaction conditions and product yields are shown in Tables 1 and 2.

References

[1] Tetrahedron, 2016, vol. 72, # 5, p. 734 - 745

5-bromo-1-methyl-1H-indole-3-carboxylicacid Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

5-bromo-1-methyl-1H-indole-3-carboxylicacid Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Adamas Reagent, Ltd.
Tel
400-6009262 15618770481
Fax
021-64823266
Email
yhx@titansci.com
Country
China
ProdList
14101
Advantage
59
Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
13761987713
Fax
021 51613951
Email
hxzheng@sunwaypharm.cn
Country
China
ProdList
8667
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
7245
Advantage
62
Wuhan TCASChem Technology Co., Ltd.
Tel
027-86697669 13986148687
Fax
86-027-86697669
Email
sales@tcaschem.com
Country
China
ProdList
4000
Advantage
55
Thermo Fisher Scientific
Tel
800-810-5118
Fax
+86-10-84193589
Email
cnchemical@thermofisher.com
Country
China
ProdList
17770
Advantage
75
Shanghai Witofly Chemical Co.,Ltd
Tel
Email
sales@witofly.com
Country
China
ProdList
2864
Advantage
52
Bide Pharmatech Ltd.
Tel
400-400-164-7117 18317119277
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
40000
Advantage
60
Porse Fine Chemical Co.,LTD
Tel
20-66003216 18666003216
Fax
+86-20-28069063
Email
info@porsefinechemical.com
Country
China
ProdList
1941
Advantage
62

400071-95-6, 5-bromo-1-methyl-1H-indole-3-carboxylicacidRelated Search:


  • 5-bromo-1-methyl-1H-indole-3-carboxylicacid
  • 5-Bromo-1-methylindole-3-carboxylic acid
  • 1H-Indole-3-carboxylic acid, 5-bromo-1-methyl-
  • 400071-95-6