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Bicyclo[2.2.1]heptan-2-one, 7-(bromomethyl)-1,7-dimethyl-, anti- is a complex organic compound with the chemical formula C10H15BrO. It is a derivative of bicyclo[2.2.1]heptan-2-one, featuring a bromine atom attached to the methyl group at the 7th position and a methyl group at the 1st position. The "anti" descriptor indicates the relative stereochemistry of the substituents at the 1st and 7th positions, which are on opposite sides of the ring. Bicyclo[2.2.1]heptan-2-one, 7-(bromomethyl)-1,7-dimethyl-, anti- is characterized by its unique molecular structure and may have potential applications in the synthesis of pharmaceuticals or other organic compounds due to its reactive bromine atom and cyclic structure.

2111-66-2

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2111-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2111-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,1 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2111-66:
(6*2)+(5*1)+(4*1)+(3*1)+(2*6)+(1*6)=42
42 % 10 = 2
So 2111-66-2 is a valid CAS Registry Number.

2111-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-8-bromo-bornan-2-one

1.2 Other means of identification

Product number -
Other names (+/-)-8-Brom-bornan-2-on

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 -
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More Details:2111-66-2 SDS

2111-66-2Relevant 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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