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214915-69-2

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214915-69-2 Usage

General Description

4-BROMO-7-METHYLTRYPTOPHOL is a chemical compound that belongs to the class of tryptophol derivatives. It is a derivative of tryptophol, which is a natural compound found in certain organisms. The presence of a bromine atom in the 4th position and a methyl group in the 7th position distinguishes this compound from tryptophol. 4-BROMO-7-METHYLTRYPTOPHOL has potential applications in medicinal chemistry and drug development due to its structure and biological activity. It can be used as a building block for the synthesis of new drugs or as a research tool in the study of biological pathways and processes involving tryptophol and its derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 214915-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,9,1 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214915-69:
(8*2)+(7*1)+(6*4)+(5*9)+(4*1)+(3*5)+(2*6)+(1*9)=132
132 % 10 = 2
So 214915-69-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H12BrNO/c1-7-2-3-9(12)10-8(4-5-14)6-13-11(7)10/h2-3,6,13-14H,4-5H2,1H3

214915-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromo-7-methyl-1H-indol-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names 4-bromo-7-methyl tryptophol

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:214915-69-2 SDS

214915-69-2Downstream Products

214915-69-2Relevant articles and documents

Process for the scalable synthesis of 1,3,4,9-tetrahydropyrano[3,4-b]-indole derivatives

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Page/Page column 7-8, (2010/10/20)

The invention is directed to a process of synthesizing compounds of formula (VI): wherein R1-R9, R3′, R4′ and Y are as set forth in the specification, and said method is useful for large scale synthesis thereof.

R-ENANTIOMERS OF PYRANOINDOLE DERIVATIVES AGAINST HEPATITIS C

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Page 23-24, (2008/06/13)

The invention is directed to a compound and a pharmaceutical composition of the formula: Wherein substitutions at R1, R2, R3 - R12, and Y are set forth in the specification.

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