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tert-butyloxycarbonyl-glycyl-dehydrophenylalaninamide-N-methyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124194-25-8

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124194-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124194-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,1,9 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 124194-25:
(8*1)+(7*2)+(6*4)+(5*1)+(4*9)+(3*4)+(2*2)+(1*5)=108
108 % 10 = 8
So 124194-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H23N3O4/c1-17(2,3)24-16(23)19-11-14(21)20-13(15(22)18-4)10-12-8-6-5-7-9-12/h5-10H,11H2,1-4H3,(H,18,22)(H,19,23)(H,20,21)/b13-10-

124194-25-8SDS

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 tert-butyl N-[2-[[(Z)-3-(methylamino)-3-oxo-1-phenylprop-1-en-2-yl]amino]-2-oxoethyl]carbamate

1.2 Other means of identification

Product number -
Other names tert-Butyloxycarbonyl-glycyl-dehydrophenylalaninamide-N-methyl

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:124194-25-8 SDS

124194-25-8Downstream Products

124194-25-8Relevant academic research and scientific papers

Impact of the ΔPhe configuration on the Boc-Gly-ΔPhe-NHMe conformation: experiment and theory

Buczek, Aneta,Siod?ak, Dawid,Bujak, Maciej,Makowski, Maciej,Kupka, Teobald,Broda, Ma?gorzata A.

, p. 1685 - 1697 (2019/07/29)

Conformational propensities of N-t-butoxycarbonyl-glycine-(E/Z)-dehydrophenylalanine N′-methylamides (Boc-Gly-(E/Z)-ΔPhe-NHMe) in chloroform were investigated by NMR and IR techniques. The low-temperature crystal structure of the E isomer was determined b

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