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2-chloro-1,7,7-trimethyl-2-nitrobicyclo[2.2.1]heptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75107-65-2

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75107-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75107-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75107-65:
(7*7)+(6*5)+(5*1)+(4*0)+(3*7)+(2*6)+(1*5)=122
122 % 10 = 2
So 75107-65-2 is a valid CAS Registry Number.

75107-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-4,7,7-trimethyl-3-nitrobicyclo[2.2.1]heptane

1.2 Other means of identification

Product number -
Other names 2-Chloro-2-nitrocamphane

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:75107-65-2 SDS

75107-65-2Downstream Products

75107-65-2Relevant academic research and scientific papers

New Reagents for the Synthesis of gem-Halonitro Compounds from Oximes

Walters, Thomas R.,Zajac, Walter W.,Woods, James M.

, p. 316 - 321 (2007/10/02)

The utility of the N-haloheterocycles 1-sodio-3,5-dichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (4), 1,3,5-trichloro-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (5), 1,3-dibromo-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (6), and 1,3-dibromo-5,5-dimethylhydantoin (

AN EFFECTIVE AND MILD METHOD FOR THE CONVERSION OF OXIMES TO SECONDARY NITRO COMPOUNDS

Corey, E. J.,Estreicher, Herbert

, p. 1117 - 1120 (2007/10/02)

A mild and efficient process for the conversion of cyclic ketones to staurated nitro compounds, as outlined in eq. 1 below, is described.

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