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N-acetyl-5-hydroxy-L-tryptophan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67010-10-0

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67010-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67010-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67010-10:
(7*6)+(6*7)+(5*0)+(4*1)+(3*0)+(2*1)+(1*0)=90
90 % 10 = 0
So 67010-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2O4/c1-7(16)15-12(13(18)19)4-8-6-14-11-3-2-9(17)5-10(8)11/h2-3,5-6,12,14,17H,4H2,1H3,(H,15,16)(H,18,19)/t12-/m0/s1

67010-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-acetamido-3-(5-hydroxy-1H-indol-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names L-Tryptophan,N-acetyl-5-hydroxy

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:67010-10-0 SDS

67010-10-0Downstream Products

67010-10-0Relevant academic research and scientific papers

Dipeptides of L-5-hydroxytryptophan, processes for their preparation and drugs in which they are present

-

, (2008/06/13)

The present invention relates to new dipeptides of L-5-hydroxytryptophan. They correspond to the general formula below: STR1 in which: X represents hydrogen or a lower acyl radical and Q represents a free or esterified aminoacid radical. Application: drugs for combating disorder of the serotoninergic system.

Syntheses of Substituted L- and D-Tryptophans

Irie, Kunihiko,Ishida, Akihiko,Nakamura, Tohru,Oh-ishi, Tokuro

, p. 2126 - 2139 (2007/10/02)

Several 5-substituted nb-methoxycarbonyl-L- and -D-tryptophan derivatives were synthesized from proline by a new route involving electrochemical oxidation, as well as by the known procedures.Removal of the Nb-methoxycarbonyl group was accomplished by treatment with Me3SiI in refluxing chloroform, then alkaline hydrolysis of the methyl esters afforded 5-substituted L- and D-tryptophans with high optical purities.Keywords - L-tryptophan 5-substituted; D-tryptophan 5-substituted; anodic oxidation; N-methoxycarbonyl group deprotection; Fischer indole synthesis; iodotrimethylsilane

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