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Cyclohexanesulfonamide,2-oxo-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96355-25-8

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96355-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96355-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,5 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96355-25:
(7*9)+(6*6)+(5*3)+(4*5)+(3*5)+(2*2)+(1*5)=158
158 % 10 = 8
So 96355-25-8 is a valid CAS Registry Number.

96355-25-8SDS

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 2-oxocyclohexanesulfonamide

1.2 Other means of identification

Product number -
Other names 2-Oxo-cyclohexanesulfonic acid amide

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:96355-25-8 SDS

96355-25-8Relevant academic research and scientific papers

BRANCHED OXATHIAZINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, USE THEREOF AS MEDICINE AND DRUG CONTAINING SAID DERIVATIVES AND USE THEREOF

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Paragraph 0384-0386, (2014/02/15)

The invention relates to compounds of formula (I) and to the physiologically compatible salts thereof. Said compounds are suitable, for example, for treating hyperglycemia.

Synthesis and fungicidal activity of novel 2-oxocycloalkylsulfonylureas

Li, Xing-Hai,Yang, Xin-Ling,Ling, Yun,Fan, Zhi-Jin,Liang, Xiao-Mei,Wang, Dao-Quan,Chen, Fu-Heng,Li, Zheng-Ming

, p. 2202 - 2206 (2007/10/03)

A series of 2-oxocycloalkylsulfonylureas (2) have been synthesized in a six-step, three-pot reaction sequence from readily available cyclododecanone, cycloheptanone, and cyclohexanone. Their structures were confirmed by IR, 1H NMR, and elemental analysis. The bioassay indicated that some of them possess certain fungicidal activity against Gibberella zeae Petch. In general, compounds containing a 12-membered ring (2A) are more active than those containing a 6- or 7-membered ring (2B, 2C). In the series 2A, the compounds in which R is a disubstituted phenyl or pyrimidyl showed better activity than those in which R is a monosubstituted phenyl or pyrimidyl, and aryl-substituted compounds have somewhat higher activity than those substituted by pyrimidyl. The further bioassay showed that the representative of 2A, 2A15, has good fungicidal activities against not only G. zeae Petch but also Botrytis cinerea Pers, Colletotrichum orbiculare Arx, Pythium aphanidermatum Fitzp, Fusarium oxysporum Schl. f. sp. Vasinfectum, etc.

2-ketosulfonamides and process for their preparation

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, (2008/06/13)

The invention relates to new 2-ketosulfonamides of the formula STR1 and to a process for their preparation, wherein the reaction mixtures obtained by reacting enamines of the formula STR2 with sulfamoyl halides of the formula STR3 are hydrolyzed to the 2-

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