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5827-57-6

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5827-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5827-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5827-57:
(6*5)+(5*8)+(4*2)+(3*7)+(2*5)+(1*7)=116
116 % 10 = 6
So 5827-57-6 is a valid CAS Registry Number.
InChI:InChI=1/3C12H25.ClH.Sn/c3*1-3-5-7-9-11-12-10-8-6-4-2;;/h3*1,3-12H2,2H3;1H;/q;;;;+1/p-1/rC36H75ClSn/c1-4-7-10-13-16-19-22-25-28-31-34-38(37,35-32-29-26-23-20-17-14-11-8-5-2)36-33-30-27-24-21-18-15-12-9-6-3/h4-36H2,1-3H3

5827-57-6SDS

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 chloro(tridodecyl)stannane

1.2 Other means of identification

Product number -
Other names Chlor-tridodecyl-stannan

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:5827-57-6 SDS

5827-57-6Downstream Products

5827-57-6Relevant articles and documents

RECYCLING OF ORGANOTIN COMPOUNDS

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Page/Page column 29; 37, (2013/12/03)

A method for the synthesis of a first organic molecule, said method comprising the steps of: a) Reacting a first reactant with an organotin reactant having at least one optionally substituted organic group having from 5 to 20 carbon atoms selected from alkyl, alkenyl, alkynyl, alkoxyalkyl, alkoxy, alkylthioalkyl, carboxylates and alkylaminoalkyl groups, thereby forming a mixture of a product and a tin-containing by-product, and b) Removing most of the tin-containing by-product from said mixture in such a way as to provide a purified product comprising less than 1000 ppm of remaining tin-containing by- product, wherein said step of removing most of said tin-containing by-product is either an extraction between a first liquid and a second liquid, said second liquid being more polar than said first liquid and at least partly immiscible therewith or is a reversed phase chromatography.

Process for the preparation of mono- and dialkyltin halogen compounds and use thereof

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Page/Page column 4-5, (2008/06/13)

Production of mixtures of monoalkyl tin trichlorides (I) and dialkyl tin dichlorides (II) by reacting tin tetrachloride with an alkyl aluminum compound in the form of an ether donor complex comprises using an amount of ether in excess of that required to form the complex. Independent claims are also included for: (1) mixtures of (I) and (II) produced as above in a yield of at least 90 mole% based on tin tetrachloride; (2) mixtures of (I) and (II) comprising at least 50 mole% (I); (3) mixtures of (I) and (II) comprising up to 5 mole% trialkyl tin chlorides; (4) mixtures of (I) and (II) comprising at least 50 mole% (I), at least 20 mole% (II) and up to 5 mole% trialkyl tin chloride.

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