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METHYL 3-(1H-PYRAZOL-1-YLMETHYL)BENZOATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

562803-63-8

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562803-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 562803-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,8,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 562803-63:
(8*5)+(7*6)+(6*2)+(5*8)+(4*0)+(3*3)+(2*6)+(1*3)=158
158 % 10 = 8
So 562803-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c1-16-12(15)11-5-2-4-10(8-11)9-14-7-3-6-13-14/h2-8H,9H2,1H3

562803-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(pyrazol-1-ylmethyl)benzoate

1.2 Other means of identification

Product number -
Other names methyl 3-(pyrazolylmethyl)benzoate

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:562803-63-8 SDS

562803-63-8Relevant academic research and scientific papers

Suzuki-miyaura cross-coupling of potassium trifluoro(N -methylheteroaryl) borates with aryl and heteroaryl halides

Molander, Gary A.,Ryu, Daweon,Hosseini-Sarvari, Mona,Devulapally, Rammohan,Seapy, Dave G.

, p. 6648 - 6656 (2013/07/26)

The synthesis of potassium trifluoro(N-methylheteroaryl)borates and their use in cross-coupling reactions with various aryl and heteroaryl halides to construct N-methyl heteroaryl-substituted aromatic and heteroaromatic compounds are reported.

A structure-Permeability study of small drug-like molecules

Fichert, Thomas,Yazdanian, Mehran,Proudfoot, John R.

, p. 719 - 722 (2007/10/03)

A systematic structure-permeability relationship study on a set of small drug-like molecules with log D values in the range -2.5 to 3 and carrying a diverse array of functionality reveals that the compounds with log D>0 and 3 are highly permeable. Surprisingly, several tetrazole derivatives were found to be substrates for efflux pump(s).

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