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100465-39-2

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100465-39-2 Usage

Type

Bicyclic enamine

Uses

Intermediate in synthesis of pharmaceuticals and other organic compounds

Reactivity

Versatile reactivity, can undergo oxidation, reduction, and addition reactions

Applications

Production of anti-inflammatory drugs, antibiotics, and other bioactive compounds

Other uses

Academic research, building block for synthesis of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 100465-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,6 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100465-39:
(8*1)+(7*0)+(6*0)+(5*4)+(4*6)+(3*5)+(2*3)+(1*9)=82
82 % 10 = 2
So 100465-39-2 is a valid CAS Registry Number.

100465-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Vinyl-2-azabicyclo[2.2.0]hex-5-en-3-one

1.2 Other means of identification

Product number -
Other names -

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:100465-39-2 SDS

100465-39-2Upstream product

100465-39-2Downstream Products

100465-39-2Relevant articles and documents

Photoreactions of Alkylated 2-Pyridones

Matsushima, Ryoka,Terada, Kazuhide

, p. 1445 - 1448 (2007/10/02)

Photoisomerisation and dimerisation reactions in solution have been studied with a series of alkylated 2-pyridones (1).The low quantum efficiencies for the photoisomerisation (0.01-0.07) are related to the short-lived singlet excited states (below 1 ns).The effects of temperature, solvent, and substrate concentration were also examined.The photodimerisation reactions of (1) are considered to involve preliminary association via strong dipole-dipole interaction rather than hydrogen-bonded pairing.

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