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3401-01-2

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3401-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3401-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3401-01:
(6*3)+(5*4)+(4*0)+(3*1)+(2*0)+(1*1)=42
42 % 10 = 2
So 3401-01-2 is a valid CAS Registry Number.

3401-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-ylcyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1-Isopropyl-cyclohexan-2,6-dion

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:3401-01-2 SDS

3401-01-2Relevant articles and documents

1,3-CYCLOHEXANEDIONE DERIVATIVES AND 1,3-CYCLOPENTANEDIONE DERIVATIVES AS BUFFERING MOLECULES IN NON-AQUEOUS SOLUTIONS

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Paragraph 0055, (2021/04/23)

This invention relates to 1,3-cyclohexanedione derivatives and 1,3-cyclopentanedione derivatives that have buffering function in non-aqueous solutions and to the use thereof for tuning the conditions to control chemical events in non-aqueous solutions. One aspect of the invention is a method for buffering a non-aqueous solution, including adding a buffering molecule to the non-aqueous solution, in which the non-aqueous solution contains an organic solvent, the buffering molecule is a 1,3-cyclohexanedione derivative or a 1,3-cyclopentanedione derivative, and the buffering molecule is optionally conjugated to a solid support.

A Conformationally Defined 6-s-trans-Retinoic Acid Isomer: Synthesis, Chemopreventive Activity, and Toxicity

Vaezi, Michael F.,Alam, Muzaffar,Sani, Brahma P.,Rogers, Tina S.,Simpson-Herren, Linda,et al.

, p. 4499 - 4507 (2007/10/02)

A conformationally defined retinoic acid analog (1) which contains a dimethylene bridge to maintain the 6-s-trans orientation for two terminal double bonds in the polyene chain was synthesized.A Reformatsky reaction was utilized to extend the polyene chai

2-Methyl-5-tert-butylcyclohexane-1,3-dione and Related 2-Alkylcyclohexane-1,3-diones from 1,3-Dimethoxybenzenes

Sardina, F. Javier,Johnston, Allen D.,Mourino, Antonio,Okamura, William H.

, p. 1576 - 1578 (2007/10/02)

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