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141261-62-3

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141261-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141261-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141261-62:
(8*1)+(7*4)+(6*1)+(5*2)+(4*6)+(3*1)+(2*6)+(1*2)=93
93 % 10 = 3
So 141261-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H27N7O6/c21-13(7-4-8-24-20(22)23)18(32)25-10-16(29)26-14(9-17(30)31)19(33)27-15(11-28)12-5-2-1-3-6-12/h1-7,11,13-15H,8-10,21H2,(H,25,32)(H,26,29)(H,27,33)(H,30,31)(H4,22,23,24)/b7-4+/t13-,14-,15+/m0/s1

141261-62-3SDS

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 (3S)-3-[[2-[[(E,2S)-2-amino-5-(diaminomethylideneamino)pent-3-enoyl]amino]acetyl]amino]-4-oxo-4-[[(1S)-2-oxo-1-phenylethyl]amino]butanoic acid

1.2 Other means of identification

Product number -
Other names Cyclic arginyl-glycyl-aspartyl-phenylglycyl

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:141261-62-3 SDS

141261-62-3Downstream Products

141261-62-3Relevant articles and documents

Sequence Dependence in Solid-Phase-Synthesis-Cyclization-Cleavage for Cyclo(-arginyl-glycyl-aspartyl-phenylglycyl-)

Nishino, Norikazu,Xu, Ming,Mihara, Hisakazu,Fujimoto, Tsutomu,Ueno, Yukio,Kumagai, Hiromichi

, p. 1479 - 1482 (2007/10/02)

A cyclic tetrapeptide with inhibitory activity toward cell adhesion, cyclo(-Arg-Gly-Asp-Phe-) (phg, phenylglycine) (IC50 = 10 μM), was synthesized.The cyclization-cleavage of the protected precursor from the oxime resin significantly depended on the sequences of the linear tetrapeptides assembled by solid-phase-synthesis on the resin. Key words: peptide synthesis; oxime resin; solid-phase-synthesis and cyclization-cleavage; cyclic tetrapeptide; Arg-Gly-Asp sequence.

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