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56909-12-7

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56909-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56909-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56909-12:
(7*5)+(6*6)+(5*9)+(4*0)+(3*9)+(2*1)+(1*2)=147
147 % 10 = 7
So 56909-12-7 is a valid CAS Registry Number.

56909-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-methylpropane-1-sulfinate

1.2 Other means of identification

Product number -
Other names Isobutyl-sulfinsaeure-methylester

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:56909-12-7 SDS

56909-12-7Relevant articles and documents

COMPOSITION, SYNTHESIS, AND USE OF NEW ARYLSULFONYL ISONITRILES

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Paragraph 0159, (2015/09/23)

This invention relates to novel isonitriles, including arylsulfonyl isonitriles, and methods for their synthesis. The isonitriles include a conjugated ring system. The structure is designed with the flexibility to have multiple substitution patterns. The isonitriles may be used in applications including, but not limited to, pharmaceutical compositions.

Methyl sulfinates as electrophiles in friedel-crafts reactions. Synthesis of aryl sulfoxides

Yuste, Francisco,Hernandez Linares, Angelica,Mastranzo, Virginia M.,Ortiz, Benjamin,Sanchez-Obregon, Ruben,Fraile, Alberto,Garcia Ruano, Jose Luis

scheme or table, p. 4635 - 4644 (2011/07/29)

The Friedel-Crafts reaction of methyl alkyl- and arylsulfinates with aromatic systems, activated by one or more electron-donating substituents (OH, OMe, NHR, NR2), provides alkyl aryl and diaryl sulfoxides under mild conditions and in moderate to good yields. The very high regioselectivity usually observed in these sulfinylation reactions is rationalized on the basis of a Wheland intermediate having a trigonal bypyramidal structure in which steric and electronic interactions are significant factors strongly destabilizing the attack to the ortho positions.

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