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30933-69-8

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30933-69-8 Usage

General Description

Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate is a chemical compound with the molecular formula C13H13BrNO3. It is a derivative of indole with a bromine and a methoxy group attached to it, and an ethyl ester group at the 2-carboxylate position. ETHYL 4-BROMO-5-METHOXY-1H-INDOLE-2-CARBOXYLATE is commonly used in organic synthesis and pharmaceutical research, as it has potential biological activity and is often studied for its potential medicinal and therapeutic applications. It is a light yellow to brown crystalline solid at room temperature, and its properties and reactivity make it a versatile intermediate in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 30933-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30933-69:
(7*3)+(6*0)+(5*9)+(4*3)+(3*3)+(2*6)+(1*9)=108
108 % 10 = 8
So 30933-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12BrNO3/c1-3-17-12(15)9-6-7-8(14-9)4-5-10(16-2)11(7)13/h4-6,14H,3H2,1-2H3

30933-69-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-bromo-5-methoxy-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 4-bromo-5-methoxy-indole-2-carboxylic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30933-69-8 SDS

30933-69-8Relevant articles and documents

SUBSTITUTED TRICYCLIC ACID DERIVATIVES AS S1P1 RECEPTOR AGONISTS USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS

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Page/Page column 47, (2011/07/08)

The present invention relates to certain substituted tricyclic acid derivatives of Formula (I) and pharmaceutically acceptable salts thereof, which exhibit useful pharmacological properties, for example, as agonists of the S1P1 receptor. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of S1P1-associated disorders, for example, psoriasis, rheumatoid arthritis, Crohn's disease, transplant rejection, multiple sclerosis, systemic lupus erythematosus, ulcerative colitis, type I diabetes, acne, myocardial ischemia-reperfusion injury, hypertensive nephropathy, glomerulosclerosis, gastritis, polymyositis, thyroiditis, vitiligo, hepatitis, biliary cirrhosis, microbial infections and associated diseases, viral infections and associated diseases, diseases and disorders mediated by lymphocytes, auto immune diseases, inflammatory diseases, and cancer.

REGIOSELECTIVE BROMINATION OF METHOXY DERIVATIVES OF ETHYL INDOLE-2-CARBOXYLATE

Tani, Masanobu,Ikegami, Hiroyo,Tashiro, Mayumi,Hiura, Tetsuji,Tsukioka, Hiroko,et al.

, p. 2349 - 2362 (2007/10/02)

Bromination of ethyl methoxyindole-2-carboxylate (1) with bromine in acetic acid proceeded on the benzene moiety of 1, whereas the reaction of 1 with pyridinium bromide perbromide in pyridine or N-bromosuccinimide in dimethylformamide gave ethyl 3-bromo-m

Ergoline synthons. 2. Synthesis of 1,5-dihydrobenz[cd]indol-4(3H)-ones and 1,3,4,5-tetrahydrobenz[cd]indol-4-amines

Kruse,Meyer

, p. 4761 - 4768 (2007/10/02)

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