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Benzenemethanol, 6-bromo-a-3-cyclopenten-1-yl-2,3-difluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

922166-16-3

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922166-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922166-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,1,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 922166-16:
(8*9)+(7*2)+(6*2)+(5*1)+(4*6)+(3*6)+(2*1)+(1*6)=153
153 % 10 = 3
So 922166-16-3 is a valid CAS Registry Number.

922166-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-Bromo-2,3-difluoro-phenyl)-cyclopent-3-enyl-methanol

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:922166-16-3 SDS

922166-16-3Relevant academic research and scientific papers

Enantioselective synthesis of nicotinic receptor probe 7,8-difluoro-1,2,3, 4,5,6-hexahydro-1,5-methano-3-benzazocine

Bashore, Crystal G.,Vetelino, Michael G.,Wirtz, Michael C.,Brooks, Paige R.,Frost, Heather N.,McDermott, Ruth E.,Whritenour, David C.,Ragan, John A.,Rutherford, Jennifer L.,Makowski, Teresa W.,Brenek, Steven J.,Coe, Jotham W.

, p. 5947 - 5950 (2007/10/03)

(Chemical Equation Presented) The development of a concise enantioselective synthesis of nicotinic alkaloid 1 is presented. The route features the synthesis and use of a "stable" aliphatic triflate 21 in an alkylation step to generate Heck precursor 24 and an enantioselective cyclization to establish a compound with the key [3.2.1]-bicyclic core, 29.

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