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L-TRP-GLY AMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38689-27-9

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38689-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38689-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,8 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38689-27:
(7*3)+(6*8)+(5*6)+(4*8)+(3*9)+(2*2)+(1*7)=169
169 % 10 = 9
So 38689-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N4O2/c14-10(13(19)17-7-12(15)18)5-8-6-16-11-4-2-1-3-9(8)11/h1-4,6,10,16H,5,7,14H2,(H2,15,18)(H,17,19)/t10-/m0/s1

38689-27-9SDS

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 (S)-2-amino-N-(2-amino-2-oxoethyl)-3-(1H-indol-3-yl)propanamide

1.2 Other means of identification

Product number -
Other names Pksi 527

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:38689-27-9 SDS

38689-27-9Relevant academic research and scientific papers

SYNTHESIS AND CONFORMATION OF N-TRITYL DIPEPTIDE DERIVATIVES

Matsoukas, J.,Tsegenidis, Th.,Cordopatis, P.,Theodoropoulos, D.

, p. 1869 - 1872 (2007/10/02)

N-Tritylamino acids activated with DCC/HOBt, were coupled with various amino acid derivatives without racemization.The trityl group was split off quantitatively in 10percent CCl3COOH monohydrate or CH2ClCOOH in CH2Cl2

Synthesis and some pharmacological properties of [8-L-tryptophan]oxytocin.

Bodanszky,Tolle,Seto,Sawyer

, p. 1259 - 1261 (2007/10/02)

Condensation of (tert-butyloxycarbonyl)tocinoic acid with L-prolyl-L-tryptophylglycinamide produced the Boc derivative of a nonapeptide (disulfide) which on deprotection afforded [8-L-tryptophan]oxytocin. In assays on the rat uterus in vitro and in vivo t

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