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2,6-Diazabicyclo[2.2.0]hex-5-en-3-one, 1,2,5-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76599-91-2

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76599-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76599-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,9 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76599-91:
(7*7)+(6*6)+(5*5)+(4*9)+(3*9)+(2*9)+(1*1)=192
192 % 10 = 2
So 76599-91-2 is a valid CAS Registry Number.

76599-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,6-trimethyl-3,5-diazabicyclo[2.2.0]hex-5-en-2-one

1.2 Other means of identification

Product number -
Other names 1,3,6-trimethyl-2,6-diazabicyclo<2.2.0>hex-2-en-5-one

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:76599-91-2 SDS

76599-91-2Relevant academic research and scientific papers

Photochemistry of 2,3,6-Trialkyl-4-pyrimidinones in Liquid Ammonia-Ether Solution. Chemistry of Dewar 4-Pyrimidinones

Hirokami, Shun-ichi,Takahashi, Tamiko,Nagata, Masanori,Hirai, Yoshiro,Yamazaki, Takao

, p. 1769 - 1777 (1981)

Irradiation of the 2,3,6-trialkyl-4-pyrimidinones 4 and 18 in liquid ammonia-ether (7:3) solution at -40 deg C gave the corresponding Dewar 4-pyrimidinones, 5 and 19, which decomposed in inert solvents at room temperature and did not revert to the corresponding 4-pyrimidinones.The first-order rate constants for disappearance of 5 and 19 were measured at 10-54 deg C.The solvolysis reactions of 5 and 19 occur in methanol to give the α-(aminoethylidene)-β-methoxy-β-lactams 6 and 20, respectively, whereas treatment of 5 and 19 in methanol containing sodium methoxide gave the imino ether 7 and the ketal 23, respectively.The reactions of 5 and 19 in methylamine-ether (1:4) solution afforded the imine derivatives 9 and 24, respectively.Furthermore, treatment of 5 in methanol-d containing sodium methoxide gave N-methyl-3--2-butenamide-2-d (7D1) and N-methyl-3--2-butenamide-2,4-d2 (7D2) as the major components.The imino ether 7 did not give the deuterated imino ether under similar conditions.The products (7, 9, 23, 24, and 27) formed in basic solutions are discussed in terms of abstraction of the methine proton by base from the Dewar 4-pyrimidinone or in terms of addition of nucleophile to the imino group of Dewar 4-pyrimidinone.

Rearrangements of Dewar 4-Pyrimidinones and 4-methoxy-2-azetidinones. Reactions through Azetidinyl and Acyl Cations

Hirokami, Shun-ichi,Takahashi, Tamiko,Nagata, Masanori,Yamazaki, Takao

, p. 2455 - 2468 (2007/10/02)

Irradiation of 2,3,6-trialkyl-4-pyrimidinones 1 and the termal reactions of the Dewar 4-pyrimidinones 2 in aliphatic carboxylic acid solutions gave the corresponding tetraalkylpyrimidinium-5-carboxylates 3.The structures of the betaines 3 were established

Photochemistry of 4-Pyrimidinones: Isolation of Dewar Isomers

Hirokami, Shun-ichi,Takahashi, Tamiko,Kurosawa, Kazumi,Nagata, Masanori,Yamazaki, Takao

, p. 166 - 169 (2007/10/02)

The 1,3,6-trialkyl-5-oxo-2,6-diazabicyclohex-2-enes (Dewar 4-pyrimidinones) 2a-d which are formed in the photolysis of 2,3,6-trialkyl-4-pyrimidinones 1a-d were isolated in yields of 16-24percent.When 6--4-pyrimidinones 3a-c

PHOTOCHEMISTRY OF 4-PYRIMIDONES IN AQUEOUS SOLUTION. ISOLATION OF REVERSIBLE PHOTOHYDRATES

Takahashi, Tamiko,Hirokami, Shun-ichi,Nagata, Masanori,Yamazaki, Takao

, p. 3247 - 3250 (2007/10/02)

Both irradiation of 4-pyrimidinones (1a-c) and the reaction of the isolated Dewar 4-pyrimidinones (2a-c) in aqueous solution gave the corresponding photohydrates (3a-c) which reverted spontaneously to the starting 1a-c in the dark reaction.The photohydrates were isolated in crystalline form and their physical properties were determined.

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