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122833-60-7

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  • (1R)-TRANS-N,N-1,2-CYCLOHEXANEDIYLBIS-( 1,1,1-TRIFLUOROMETHANESULFONAMIDE)

    Cas No: 122833-60-7

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122833-60-7 Usage

General Description

"(1R)-TRANS-N N'-1 2-CYCLOHEXANEDIYLBIS-&" is a chemical compound with a complex and specific structure, containing a cyclohexane ring and a trans configuration. The compound is likely a chiral molecule, as indicated by the (1R) designation, meaning it has a specific orientation in space. The presence of the N and N' groups suggests the compound contains amine functional groups, which are common in organic molecules and can have various chemical properties. The compound may have potential applications in pharmaceuticals, materials, or other industries due to its unique structure and potentially useful properties. However, further information about this specific compound's characteristics and potential uses would be needed to fully understand its significance in chemical research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 122833-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,3 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122833-60:
(8*1)+(7*2)+(6*2)+(5*8)+(4*3)+(3*3)+(2*6)+(1*0)=107
107 % 10 = 7
So 122833-60-7 is a valid CAS Registry Number.

122833-60-7 Well-known Company Product Price

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  • Aldrich

  • (433721)  (1R)-trans-N,N′-1,2-Cyclohexanediylbis(1,1,1-trifluoromethanesulfonamide)  97%

  • 122833-60-7

  • 433721-1G

  • 804.96CNY

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122833-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1-trifluoro-N-[(1R,2R)-2-(trifluoromethylsulfonylamino)cyclohexyl]methanesulfonamide

1.2 Other means of identification

Product number -
Other names 2R-cyclohexane-1,2-diyl)bis(trifluoromethanesulfonamide))

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:122833-60-7 SDS

122833-60-7Relevant articles and documents

Catalytic enantioselective cyclopropanation with bis(halomethyl) zinc reagents. II. The effect of promoter structure on selectivity

Denmark, Scott E.,Christenson, Beritte L.,O'Connor, Stephen P.

, p. 2219 - 2222 (2007/10/02)

The catalytic, enantioselective cyclopropanation of cinnamyl alcohol has been accomplished with bis (iodomethyl)zinc in the presence of chiral bis(sulfonamides) derived from cyclohexanediamine. An extensive survey of diamine and sulfonamide structure has revealed a marked sensitivity to the spatial relationship of the amine groups, but only a modest dependence on the sulfonamide residue.

A Catalytic Enantioselective Reaction Using a C2-Symmetric Disulfonamide as a Chiral Ligand: Alkylation of Aldehydes Catalyzed by Disulfonamide-Ti(O-i-Pr)4-Dialkyl Zinc System

Takahashi, Hideyo,Kawakita, Takashi,Ohno, Masaji,Yoshioka, Masato,Kobayashi, Susumu

, p. 5691 - 5700 (2007/10/02)

Excellent enantioselective alkylation of aldehydes with dialkylzinc has been developed.This methodology is based on the concept of modifying the Lewis acid with a C2-symmetric, electron-withdrawing disulfonamide.The chiral Lewis acid catalysts used in the present study are the titanium complexes, prepared in-situ from disulfonamide and Ti(O-i-Pr)4.Key Words: Chiral disulfonamide; chiral titanium complex; enantioselective alkylation; dialkyl zinc; catalytic reaction

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