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82043-99-0

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82043-99-0 Usage

Compound type

Cyclic organic compound

Family

Pyrazinone

Appearance

White to light yellow crystalline powder with a faint odor

Uses

Synthesis of pharmaceuticals and agricultural chemicals

Versatility

Reactive and has functional groups for various applications

Potential applications

Medicinal chemistry (building block for bioactive molecules), intermediate in specialty chemicals and advanced materials production

Check Digit Verification of cas no

The CAS Registry Mumber 82043-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,4 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82043-99:
(7*8)+(6*2)+(5*0)+(4*4)+(3*3)+(2*9)+(1*9)=120
120 % 10 = 0
So 82043-99-0 is a valid CAS Registry Number.

82043-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5,5-Tetramethyl-5,6-dihydro-2(1H)-pyrazinone

1.2 Other means of identification

Product number -
Other names 1,2,5,6-tetrahydro-1,3,5,5-tetramethyl-2-pyrazinone

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:82043-99-0 SDS

82043-99-0Downstream Products

82043-99-0Relevant articles and documents

A Photochemical Ring Contraction of an Imino Lactam

Kleyer, Don L.,Koch, Tad H.

, p. 3145 - 3148 (2007/10/02)

The photochemical rearrangement of three tetrahydro-2-pyrazinones in aqueous medium to imidazol-5-ones is described. 1,2,5,6-Tetrahydro-3,5,5-trimethyl-2-pyrazinone (4) gives 1,2,2,4-tetramethyl-3-imidazolin-5-one (7), 1,2,5,6-tetrahydro-3,6,6-trimethyl-2-pyrazinone (5) gives 4-methyl-5-imidazolidinone (9), and 1,2,5,6-tetrahydro-1,3,5,5-tetramethyl-2-pyrazinone (6) gives 1,4-dimethyl-5-imidazolidinone (8).A mechanism involving enediimine and isoimidazole intermediates is proposed in analogy with the mechanism for rearrangement of 5,6-dihydropyrazines to imidazoles.

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