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634889-11-5

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634889-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 634889-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,8,8 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 634889-11:
(8*6)+(7*3)+(6*4)+(5*8)+(4*8)+(3*9)+(2*1)+(1*1)=195
195 % 10 = 5
So 634889-11-5 is a valid CAS Registry Number.

634889-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[benzyl-[(4-chlorophenyl)methyl]amino]acetonitrile

1.2 Other means of identification

Product number -
Other names Acetonitrile,[[(4-chlorophenyl)methyl](phenylmethyl)amino]

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:634889-11-5 SDS

634889-11-5Relevant articles and documents

Allosteric functional switch of neurokinin A-mediated signaling at the neurokinin NK2 receptor: Structural exploration

Valant, Céline,Maillet, Emeline,Bourguignon, Jean-Jacques,Bucher, Bernard,Utard, Valérie,Galzi, Jean-Luc,Hibert, Marcel

experimental part, p. 5999 - 6011 (2010/03/24)

The neurokinin NK2 receptor is known to pre-exist in equilibrium between at least three states: restinginactive, calcium-triggering, and cAMP-producing. Its endogeneous ligand, NKA, mainly induces the calcium response. Using a FRET-based assay, we have previously discovered an allosteric modulator of the NK2 receptor that has the unique ability to discriminate among the two signaling pathways: calcium-signaling is not affected while cAMP signaling is significantly decreased. A series of compounds have been prepared and studied in order to better understand the structural determinants of this allosteric functional switch of a GPCR. Most of them display the same allosteric profile, with smooth pharmacomodulation. One compound however exhibits significantly improved modulatory properties of NKA induced signaling when compared to the original modulator. 2009 American Chemical Society.

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