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166953-64-6

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166953-64-6 Usage

Description

BENZYL 4-BROMOTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE is a chemical compound belonging to the pyridinecarboxylate class, characterized by its molecular formula C14H16BrNO2. It is a white to off-white crystalline powder that serves as a crucial pharmaceutical intermediate, playing a significant role in the synthesis of various pharmaceutical drugs.
Used in Pharmaceutical Industry:
BENZYL 4-BROMOTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE is used as a pharmaceutical intermediate for the production of active pharmaceutical ingredients (APIs). Its potential biological activity and importance as a building block in the synthesis of many pharmaceuticals make it a valuable component in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 166953-64-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,5 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 166953-64:
(8*1)+(7*6)+(6*6)+(5*9)+(4*5)+(3*3)+(2*6)+(1*4)=176
176 % 10 = 6
So 166953-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16BrNO2/c14-12-6-8-15(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5,12H,6-10H2

166953-64-6 Well-known Company Product Price

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  • Aldrich

  • (569224)  4-Bromo-N-Z-piperidine  96%

  • 166953-64-6

  • 569224-1G

  • 462.15CNY

  • Detail
  • Aldrich

  • (569224)  4-Bromo-N-Z-piperidine  96%

  • 166953-64-6

  • 569224-5G

  • 1,552.59CNY

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166953-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl 4-bromopiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names Benzyl 4-bromotetrahydro-1(2H)-pyridinecarboxylate

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:166953-64-6 SDS

166953-64-6Relevant articles and documents

Copper-Catalyzed Reductive Cross-Coupling of Nonactivated Alkyl Tosylates and Mesylates with Alkyl and Aryl Bromides

Liu, Jing-Hui,Yang, Chu-Ting,Lu, Xiao-Yu,Zhang, Zhen-Qi,Xu, Ling,Cui, Mian,Lu, Xi,Xiao, Bin,Fu, Yao,Liu, Lei

supporting information, p. 15334 - 15338 (2016/02/18)

A copper-catalyzed reductive cross-coupling reaction of nonactivated alkyl tosylates and mesylates with alkyl and aryl bromides was developed. It provides a practical method for efficient and cost-effective construction of aryl-alkyl and alkyl-alkyl C=C bonds with stereocontrol from readily available substrates. When used in an intramolecular fashion, the reaction enables convenient access to various substituted carbo- or heterocycles, such as 2,3-dihydrobenzofuran and benzochromene derivatives.

1-(4-PIPERIDINYL) BENZIMIDAZOLONES AS HISTAMINE H3 ANTAGONISTS

-

Page 44-45, (2010/02/04)

Disclosed are histamine H3 antagonists of the formula (I) wherein R1 is benzimidazolone derivative, M1 and M2 are optionally substituted carbon or nitrogen, R2 includes optionally substituted aryl or heteroaryl, and the remaining variables are as defined

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