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787549-26-2

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787549-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 787549-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,7,5,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 787549-26:
(8*7)+(7*8)+(6*7)+(5*5)+(4*4)+(3*9)+(2*2)+(1*6)=232
232 % 10 = 2
So 787549-26-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H31N3O6/c1-3-24(31)28-14-8-7-11-22(30-27(34)35-17-19-9-5-4-6-10-19)26(33)29-20-12-13-21-18(2)15-25(32)36-23(21)16-20/h4-6,9-10,12-13,15-16,22H,3,7-8,11,14,17H2,1-2H3,(H,28,31)(H,29,33)(H,30,34)/t22-/m0/s1

787549-26-2 Well-known Company Product Price

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  • Sigma

  • (M2195)  MOCPAC  ≥95% (HPLC), solid

  • 787549-26-2

  • M2195-2MG

  • 1,749.15CNY

  • Detail

787549-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[(2S)-1-[(4-methyl-2-oxochromen-7-yl)amino]-1-oxo-6-(propanoylamino)hexan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names phenylmethyl N-[(2S)-1-[(4-methyl-2-oxochromen-7-yl)amino]-1-oxo-6-(propanoylamino)hexan-2-yl]carbamate

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:787549-26-2 SDS

787549-26-2Downstream Products

787549-26-2Relevant academic research and scientific papers

Subtype selective substrates for histone deacetylases

Heltweg, Birgit,Dequiedt, Franck,Marshall, Brett L.,Brauch, Carsten,Yoshida, Minoru,Nishino, Norikazu,Verdin, Eric,Jung, Manfred

, p. 5235 - 5243 (2007/10/03)

To probe the steric requirements for deacylation, we synthesized lysine-derived small molecule substrates and examined structure-reactivity relationships with various histone deacetylases. Rat liver, human HeLa, and human recombinant class I and II histon

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