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Bicyclo[2.2.1]heptan-2-one, 7-(bromomethyl)-1,7-dimethyl- is a complex organic compound with the molecular formula C10H15BrO. It is a derivative of bicyclo[2.2.1]heptan-2-one, featuring a bromomethyl group at the 7-position and two methyl groups at the 1 and 7 positions. Bicyclo[2.2.1]heptan-2-one, 7-(bromomethyl)-1,7-dimethyl- is characterized by its bicyclic structure, with a ketone functional group at the 2-position and a bromine atom attached to a methylene group. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. Due to its unique structure and functional groups, it has potential applications in the synthesis of various organic compounds, pharmaceuticals, and agrochemicals. However, it is important to handle Bicyclo[2.2.1]heptan-2-one, 7-(bromomethyl)-1,7-dimethyl- with care, as it may have hazardous properties and require proper safety measures during its use and storage.

3751-96-0

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3751-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3751-96-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3751-96:
(6*3)+(5*7)+(4*5)+(3*1)+(2*9)+(1*6)=100
100 % 10 = 0
So 3751-96-0 is a valid CAS Registry Number.

3751-96-0SDS

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 8-bromonorbornan-2-one

1.2 Other means of identification

Product number -
Other names 8-bromo-bornan-2-one

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:3751-96-0 SDS

3751-96-0Relevant academic research and scientific papers

MICROBIAL TRANSFORMATIONS. PART 7 (1) BIOHYDROXYLATION OF BORNYLAMIDE DERIVATIVES BY THE FUNGUS BEAUVERIA SULFURESCENS

Fourneron, Jean-Dominique,Archelas, Alain,Vigne, Bernard,Furstoss, Roland

, p. 2273 - 2284 (2007/10/02)

The biohydroxylation of various amide derivatives of norbornane and of camphane have been studied, in order to explore the possible influence of this amide group configuration and substitution upon the regio, the stereo and the enantioselectivity of the p

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