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1221818-32-1

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1221818-32-1 Usage

General Description

Tert-Butyl 7-bromo-3-azabicyclo[2.2.1]heptane-3-carboxylate is a chemical compound that belongs to the class of azabicyclo compounds. It is a white, crystalline solid with a molecular formula of C12H19NO2Br and a molecular weight of 300.19 g/mol. tert-Butyl 7-broMo-3-azabicyclo[2.2.1]heptane-3-carboxylate is often used in organic synthesis and pharmaceutical research as a building block for creating more complex molecules. It is known for its sterically hindered tert-butyl group and the bromo substitution on the azabicyclo ring, which can affect its reactivity and biological activity. Overall, tert-Butyl 7-bromo-3-azabicyclo[2.2.1]heptane-3-carboxylate is a versatile chemical that has various potential applications in the field of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1221818-32-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,8,1 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1221818-32:
(9*1)+(8*2)+(7*2)+(6*1)+(5*8)+(4*1)+(3*8)+(2*3)+(1*2)=121
121 % 10 = 1
So 1221818-32-1 is a valid CAS Registry Number.

1221818-32-1SDS

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 tert-Butyl 7-bromo-3-azabicyclo[2.2.1]heptane-3-carboxylate

1.2 Other means of identification

Product number -
Other names Y7266

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:1221818-32-1 SDS

1221818-32-1Downstream Products

1221818-32-1Relevant articles and documents

Epibatidine isomers and analogues: Structure-activity relationships

White, Richard,Malpass, John R.,Handa, Sandeep,Richard Baker,Broad, Lisa M.,Folly, Liz,Mogg, Adrian

, p. 5493 - 5497 (2006)

Binding affinities for a range of epibatidine isomers and analogues at the α4β2 and α3β4 nAChR subtypes are reported; compounds having similar N-N distances to epibatidine show similar, high potencies.

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