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258264-42-5

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258264-42-5 Usage

Type of Compound

Quaternary ammonium salt

Usage

Reactant in organic synthesis and chemical research

Physical State

White to off-white solid

Solubility

Soluble in water and organic solvents

Applications

a. Precursor to pharmaceutical and agrochemical compounds
b. Potential use in asymmetric catalysis
c. Building block in organic chemistry

Unique Structure

Contains a quaternary ammonium group

Reactivity

Exhibits distinct properties useful in various chemical processes

Check Digit Verification of cas no

The CAS Registry Mumber 258264-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,2,6 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 258264-42:
(8*2)+(7*5)+(6*8)+(5*2)+(4*6)+(3*4)+(2*4)+(1*2)=155
155 % 10 = 5
So 258264-42-5 is a valid CAS Registry Number.

258264-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-bromo-1-azoniatricyclo[2.2.1.0~2,6~]heptane bromide

1.2 Other means of identification

Product number -
Other names 1-benzyl-3-bromo-1-azatricyclo[2.2.1.0^{2,6}]heptan-1-ium bromide

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:258264-42-5 SDS

258264-42-5Relevant articles and documents

7-Substituted 2-Azabicyclo[2.2.1]heptanes as key intermediates for the synthesis of novel epibatidine analogues; synthesis of syn- and anti-Isoepiboxidine

Malpass, John R.,White, Richard

, p. 5328 - 5334 (2007/10/03)

Neighboring group participation by the 2-nitrogen in anti-7-bromo-2-benzyl- 2-azabicyclo[2.2.1]heptane allows ready nucleophilic substitution at the 7-position by C, N, O, and halogen nucleophiles and opens the way to a range of novel 7-substituted 2-azab

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