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Cyclohexanone, 3,3,5,5-tetramethyl-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74609-83-9

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74609-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74609-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,0 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74609-83:
(7*7)+(6*4)+(5*6)+(4*0)+(3*9)+(2*8)+(1*3)=149
149 % 10 = 9
So 74609-83-9 is a valid CAS Registry Number.

74609-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5,5-tetramethyl-2-nitrocyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 2-nitro-3,3,5,5-tetramethylcyclohexanone

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:74609-83-9 SDS

74609-83-9Relevant academic research and scientific papers

α-Nitro Ketones. 3. Stereochemistry of the Nitration of 1-Acetoxycyclohexenes: Synthesis of 2-Nitrocyclohexanones

Oezbal, Hadi,Zajac, Walter W.

, p. 3082 - 3087 (2007/10/02)

The nitration of enol acetates of substituted cyclohexanones in acetic anhydride at 15 deg C with concentrated nitric acid is a kinetically controlled process which can lead to cis-trans-substituted 2-nitrocyclohexanones in very good yields.The stereochem

α-Nitro Ketones. 5. Synthesis of 2-Nitrocyclopentanones

Elfehail. Fadia E.,Zajac, Walter W.

, p. 5151 - 5155 (2007/10/02)

The synthesis of the trans-3-methyl-, trans-trans- and trans-cis-3,4-dimethyl-, trans-3,5,5-trimethyl-, and cis- and trans-5-methyl-2-nitrocyclopentanones was accomplished by nitration of substituted cyclopentanone enol acetates with nitric acid at 15 deg

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