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Guanidine, [3-(phenylmethoxy)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

205935-12-2

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205935-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205935-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,9,3 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 205935-12:
(8*2)+(7*0)+(6*5)+(5*9)+(4*3)+(3*5)+(2*1)+(1*2)=122
122 % 10 = 2
So 205935-12-2 is a valid CAS Registry Number.

205935-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-phenylmethoxyphenyl)guanidine

1.2 Other means of identification

Product number -
Other names -

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:205935-12-2 SDS

205935-12-2Relevant academic research and scientific papers

Design, synthesis and evaluation of potential inhibitors of HIV gp120-CD4 interactions

Boussard, Cyrille,Klimkait, Thomas,Mahmood, Naheed,Pritchard, Martin,Gilbert, Ian H.

, p. 2673 - 2676 (2007/10/03)

This paper describes an approach to prevent HIV-cell fusion by disrupting the interaction between HIV protein gp120 and CD4 receptor. The CD4 residues Phe43 and Arg59 make important interactions with gp120. Small molecule analogues were made to mimic the crucial features of these residues. The analogues were assayed using a cellular 'FIGS' assay to measure inhibition of cell fusion and caused some inhibition.

Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases

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, (2008/06/13)

The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative o thereof, wherein A, B, Ra, R1, R2, R3, and R4 are as described in the specification. These compounds are inhibitors of protein kinase, particularly inhibitors of JNK, a mammalian protein kinase involved cell proliferation, cell death and response to extracellular stimuli; Lck and Src kinase. The invention also relates to methods for producing these inhibitors. The invention also provides pharmaceutical compositions comprising the inhibitors of the invention and methods of utilizing those compositions in the treatment and prevention of various disorders.

Thiazole compounds useful as inhibitors of protein kinase

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, (2008/06/13)

The present invention provides a compound of formula I: or a pharmaceutically acceptable derivative thereof. These compounds are inhibitors of protein kinases, particularly inhibitors of GSK3, Aurora2, and Syk mammalian protein kinases. The invention also

Inhibitors of Src and Lck protein kinases

-

, (2008/06/13)

The present invention provides compounds of formula I: or a pharmaceutically acceptable derivative thereof, wherein A-B is N—O or O—N and G, R1, R2, R3, and R4 are as described in the specification. These compou

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