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120996-46-5

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120996-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120996-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,9 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 120996-46:
(8*1)+(7*2)+(6*0)+(5*9)+(4*9)+(3*6)+(2*4)+(1*6)=135
135 % 10 = 5
So 120996-46-5 is a valid CAS Registry Number.

120996-46-5SDS

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 (R)-6-Benzyloxymethyl-5,6-dihydro-2-pyrone

1.2 Other means of identification

Product number -
Other names (R)-6-Benzyloxymethyl-5,6-dihydro-pyran-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:120996-46-5 SDS

120996-46-5Relevant articles and documents

Total synthesis of (+)-aspergillide C

Kanematsu, Makoto,Yoshida, Masahiro,Shishido, Kozo

, p. 1372 - 1374 (2011/03/21)

The enantioselective total synthesis of aspergillide C, a member of a novel class of 14-membered macrolides isolated from the marine-derived fungus Aspergillus ostianus strain 01F313, has been accomplished employing a highly diastereoselective intramolecu

A Unified Procedure for Diastereo- and Enantiocontrolled Construction of Compactin Lactone and Calcitriol Enyne

Oizumi, Mitsuru,Takahashi, Michiyasu,Ogasawara, Kunio

, p. 1111 - 1113 (2007/10/03)

A unified diastereo- and enantiocontrolled entry into compactin lactone, an essential structural moiety for the biological activity of compactin, and calcitriol enyne, an A-ring precursor of calcitriol, has been developed by use of the same stereocontrol

A CONVERGENT ENANTIOCONTROLLED ROUTE TO MEVALONOLACTONE AND VITAMIN E FROM (S)-O-BENZYLGLYCIDOL

Takano, Seiichi,Shimazaki, Youichi,Iwabuchi, Yoshiharu,Ogasawara, Kunio

, p. 3619 - 3622 (2007/10/02)

A convergent enantiocontrolled route to (+) and (-)-mevalonolactones and vitamin E has been developed using (S)-O-benzylglycidol as the sole chiral block.

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