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13732-62-2

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13732-62-2 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 13732-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,3 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13732-62:
(7*1)+(6*3)+(5*7)+(4*3)+(3*2)+(2*6)+(1*2)=92
92 % 10 = 2
So 13732-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3S.C4H9NO/c1-6-2-4-7(5-3-6)11(8,9)10;1-3-6-4-2-5-1/h2-5H,1H3,(H,8,9,10);5H,1-4H2

13732-62-2 Well-known Company Product Price

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  • Aldrich

  • (28270)  CuringAgentC  ≥95.0% (NT)

  • 13732-62-2

  • 28270-500G

  • 2,110.68CNY

  • Detail

13732-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylbenzenesulfonic acid,morpholine

1.2 Other means of identification

Product number -
Other names morpholinium toluene-4-sulfonate

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:13732-62-2 SDS

13732-62-2Downstream Products

13732-62-2Relevant articles and documents

A metal-free three-component reaction for the regioselective synthesis of 1,4,5-trisubstituted 1,2,3-triazoles

Thomas, Joice,John, Jubi,Parekh, Nikita,Dehaen, Wim

supporting information, p. 10155 - 10159 (2015/03/31)

A metal-free three-component reaction to synthesize 1,4,5-trisubstituted 1,2,3-triazoles from readily available building blocks,such as aldehydes,nitroalkanes,and organic azides,is described. The process is enabled by an organocatalyzed Knoevenagel condensation of the formyl group with the nitro compound,which is followed by the 1,3-dipolar cycloaddition of the azide to the activated alkene. The reaction features an excellent substrate scope,and the products are obtained with high yield and regioselectivity. This method can be utilized for the synthesis of fused triazole heterocycles and materials with several triazole moieties.

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