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56651-57-1

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56651-57-1 Usage

Chemical Properties

clear colorless to yellow liquid

Uses

1-(isocyanatomethyl)-4-methylbenzene is a useful reactant for organic synthesis and reactions.

General Description

4-Methylbenzyl isocyanate, also known as p-methylbenzyl isocyanate, is an organic building block containing an isocyanate group. Its vapor pressure has been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 56651-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,5 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56651-57:
(7*5)+(6*6)+(5*6)+(4*5)+(3*1)+(2*5)+(1*7)=141
141 % 10 = 1
So 56651-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c1-8-2-4-9(5-3-8)6-10-7-11/h2-5H,6H2,1H3

56651-57-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (487422)  4-Methylbenzylisocyanate  97%

  • 56651-57-1

  • 487422-1G

  • 892.71CNY

  • Detail
  • Aldrich

  • (487422)  4-Methylbenzylisocyanate  97%

  • 56651-57-1

  • 487422-5G

  • 2,440.62CNY

  • Detail

56651-57-1SDS

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 4-Methylbenzyl isocyanate

1.2 Other means of identification

Product number -
Other names 1-(isocyanatomethyl)-4-methylbenzene

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:56651-57-1 SDS

56651-57-1Relevant articles and documents

COMBINED TREATMENT WITH A TLR7 AGONIST AND AN HBV CAPSID ASSEMBLY INHIBITOR

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Page/Page column 29; 30, (2018/04/13)

The present invention is directed to compositions and methods for treating hepatitis B virus infection. In particular, the present invention is directed to a combination therapy comprising administration of a TLR7 agonist and an HBV capsid assembly inhibi

Amide compound, pharmaceutical composition, preparation method and application thereof

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Paragraph 0244-0247, (2018/09/11)

The invention provides an amide compound, a pharmaceutical composition, a preparation method and application thereof and belongs to the field of medicine. Structure of the amide compound is shown as aformula I. The preparation method includes: in an alkaline condition and in an organic solvent, allowing a compound I and a compound II to be in condensation reaction. The amide compound or pharmaceutically acceptable salt thereof have long-acting sensory and/or motion blocking activity, can be used for preparing long-acting local anesthetic or analgesic and is long in efficacy lasting time, little side effect and high in medication safety.

(Tosylimino)phenyl-λ3-iodane as a reagent for the synthesis of methyl carbamates via hofmann rearrangement of aromatic and aliphatic carboxamides

Yoshimura, Akira,Luedtke, Matthew W.,Zhdankin, Viktor V.

experimental part, p. 2087 - 2091 (2012/05/05)

A new, mild procedure for the Hofmann rearrangement of aromatic and aliphatic carboxamides using (tosylimino)phenyl-λ3-iodane, PhINTs, as a reagent is reported. Because of the mild reaction conditions, this method is particularly useful for the Hofmann rearrangement of substituted benzamides, which usually afford complex reaction mixtures with other hypervalent iodine oxidants. The mild reaction conditions and high selectivity in the reaction of carboxamides with PhINTs allow the isolation of the initially formed labile isocyanates or their subsequent conversion to stable carbamates by treatment with alcohols.

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