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Pyridine, 2-[(2-chlorophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36995-37-6

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36995-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36995-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,9 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36995-37:
(7*3)+(6*6)+(5*9)+(4*9)+(3*5)+(2*3)+(1*7)=166
166 % 10 = 6
So 36995-37-6 is a valid CAS Registry Number.

36995-37-6SDS

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 2-[(2-chlorophenyl)methyl]pyridine

1.2 Other means of identification

Product number -
Other names 2-(2-Chlor-benzyl)-pyridin

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:36995-37-6 SDS

36995-37-6Relevant academic research and scientific papers

Versatile C(sp2)?C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes

Dean, William M.,?iau?iulis, Mindaugas,Storr, Thomas E.,Lewis, William,Stockman, Robert A.

supporting information, p. 10013 - 10016 (2016/08/16)

The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.

Fungicidal compounds

-

, (2008/06/13)

Fungicidal compounds having the formula (I): STR1 wherein R1 is an optionally substituted phenyl group; R2 and R3, which are the same or different, are hydrogen or C1-4 alkyl; R4, R5 and R

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