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2(1H)-Cycloheptimidazolone, 1-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144104-64-3

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144104-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144104-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144104-64:
(8*1)+(7*4)+(6*4)+(5*1)+(4*0)+(3*4)+(2*6)+(1*4)=93
93 % 10 = 3
So 144104-64-3 is a valid CAS Registry Number.

144104-64-3SDS

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 1-(4-chlorophenyl)cyclohepta[d]imidazol-2-one

1.2 Other means of identification

Product number -
Other names 1-p-chlorophenyl-1,3-diazaazulanone

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:144104-64-3 SDS

144104-64-3Downstream Products

144104-64-3Relevant academic research and scientific papers

Photoreactions of 3-tosyl- and 6-tosyldihydro-1,3-diazaazulanones to form 1,3-diazaazulanones and ionic pairs between p-toluenesulfonate anion and 1,3-diazadihydroazulanone cations

Saito, Katsuhiro,Kunisada, Tomoko,Ishiguro, Hiroyuki,Sato, Michie,Doi, Tadayuki

, p. 2315 - 2324 (2001)

A solvent effect was found on the photoreactions of 1-aryl-3-tosyldihydro-1,3-diazaazulanones with a low pressure mercury lamp. Thus, ion pairs between p-toluenesulfonate anion and the corresponding 1-aryl-1,3-diazadihydroazulanone cations were afforded b

Photoreactions of N-tosyldihydrodiazaazulanones to form diazaazulanones and ionic pairs between p-toluenesulfonate anion and tropyliumions

Doi, Tadayuki,Ishiguro, Hiroyuki,Sato, Michie,Saito, Katsuhiro

, p. 1775 - 1778 (2007/10/03)

Low pressure mercury lamp irradiations of N-aryl-N'- tosyldihydrodiazaazulanones in acetonitrile afforded the corresponding N- aryldiazaazulanones. Analogous photoreactions but using tetrahydrofuran as a solvent gave ion pairs between p-toluenesulfonate (

-TYPE CYCLOADDITION REACTIONS OF N-ARYL-2,4,6-CYCLOHEPTATRIENE-1-IMINES AND 2,4,6-CYCLOHEPTATRIENE-1-THIONE WITH p-TOLUENESULFONYL ISOCYANATE: FORMATION OF 1,3-DIAZAAZULANONES

Ito, Kazuaki,Saito, Katsuhiro,Takeuchi, Shigeyuki,Takahashi, Kensuke

, p. 1415 - 1422 (2007/10/02)

Reactions of N-aryl-2,4,6-cycloheptatriene-1-imines and 2,4,6-cycloheptatriene-1-thione with p-toluenesulfonyl isocyanate gave -type cycloadducts in good yields.Eliminations of tosyl groups and dehydrogenations of the adducts afforded 1,3-diazaazulan

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