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2280-85-5

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2280-85-5 Usage

General Description

6-Methyl-DL-tryptophan is a chemical compound that is a synthetic derivative of the amino acid tryptophan. It is used primarily in laboratory settings for research purposes. 6-METHYL-DL-TRYPTOPHAN has been studied for its potential biological and pharmacological properties, including its role in protein synthesis and its potential as a therapeutic agent. It has also been investigated for its potential use as a chiral building block in chemical synthesis. Additionally, 6-Methyl-DL-tryptophan has been examined for its potential role in the treatment of various medical conditions, although further research is needed to fully understand its potential benefits and limitations.

Check Digit Verification of cas no

The CAS Registry Mumber 2280-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2280-85:
(6*2)+(5*2)+(4*8)+(3*0)+(2*8)+(1*5)=75
75 % 10 = 5
So 2280-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O2/c1-7-2-3-9-8(5-10(13)12(15)16)6-14-11(9)4-7/h2-4,6,10,14H,5,13H2,1H3,(H,15,16)

2280-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methyl-DL-tryptophan

1.2 Other means of identification

Product number -
Other names 2-amino-3-(6-methyl-1H-indol-3-yl)propanoic acid

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:2280-85-5 SDS

2280-85-5Relevant articles and documents

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Snyder et al.

, p. 1873,1876 (1953)

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Synthesis of tryptophans

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, (2008/06/13)

The preparation of racemic and optically pure tryptophans is described. The D-enantiomers of the 6-substituted compounds possess a potent sweetening capability. Novel intermediates are also disclosed.

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