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1014-00-2

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1014-00-2 Usage

Type

Heterocyclic organic compound

Structure

Contains a 4H-pyran ring with a thione functional group and a 2-methyl-6-phenyl substituent

Applications

Potential applications in organic synthesis and pharmaceuticals

Properties

Unique structural and chemical properties

Safety

Handle and use with caution according to proper safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 1014-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1014-00:
(6*1)+(5*0)+(4*1)+(3*4)+(2*0)+(1*0)=22
22 % 10 = 2
So 1014-00-2 is a valid CAS Registry Number.

1014-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-phenyl-pyran-4-thione

1.2 Other means of identification

Product number -
Other names 2-Methyl-6-phenyl-pyran-4-thion

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:1014-00-2 SDS

1014-00-2Relevant articles and documents

Pyran Annelation: An Effective Route to a Tricyclic Dienone

Yamamoto, Makoto,Iwasa, Seiji,Takatsuka, Kenichi,Yamada, Kazutoshi

, p. 346 - 349 (2007/10/02)

A new pyran annelation reaction was investigated. 2,6-Dimethyl-4H-pyran-4-one (2) was converted to 2((p-tolylsulfonyl)methyl)-6-methyl-4H-pyran-4-one (7) which was alkylated at the C-2 methylene position regioselectively, and the p-tolylsulfonyl group can be easily eliminated with an aluminium amalgam reduction.On the other hand the pyran-4-one ring was easily transformed into an 1,5-diketone derivative.By joining and applying these selective alkylations and transformations, tricyclic dienone 22 was effectively synthesized from 2.

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