122833-58-3

• 

• Basic information

  1. Product Name: (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE
  2. Synonyms: N,N'-((1R,2R)-cyclohexane-1,2-diyl)diMethanesulfonaMide;N,N'-(1R,2R)-1,2-Cyclohexanediylbismethanesulfonamide;(1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE
  3. CAS NO:122833-58-3
  4. Molecular Formula: C₈H₁₈N₂O₄S₂
  5. Molecular Weight: 270.37
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 122833-58-3.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: 156-157℃
  2. Boiling Point: 428.5±55.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.36±0.1 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: Sealed in dry,Room Temperature
  8. Solubility: N/A
  9. PKA: 9.82±0.40(Predicted)
  10. CAS DataBase Reference: (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE(CAS DataBase Reference)
  11. NIST Chemistry Reference: (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE(122833-58-3)
  12. EPA Substance Registry System: (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE(122833-58-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 122833-58-3(Hazardous Substances Data)

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• (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE

  Cas No: 122833-58-3

• USD $ 3.0-3.0 / Kilogram

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• (1R,2R)-1,2-N,N'-Bis[(methane-sulfonyl)amino]-cyclohexane

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• Hangzhou J&H Chemical Co., Ltd.
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• (1R,2R)-1,2-N,N'-Bis[(methane-sulfonyl)amino]-cyclohexane

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• SAGECHEM/N,N'-((1R,2R)-cyclohexane-1,2-diyl)dimethanesulfonamide/SAGECHEM/Manufacturer in China

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• SAGECHEM LIMITED
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• (1R,2R)-1,2-N,N'-bis[(methane-sulfonyl)amino]-cyclohexane cas no. 122833-58-3 98%

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• (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE

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• N-[(1R,2R)-2-(methanesulfonamido)cyclohexyl]methanesulfonamide

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• (1R,2R)-1,2-N,N'-Bis[(methane-sulfonyl)amino]-cyclohexane 122833-58-3

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122833-58-3 Usage

General Description

(1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE is a chemical compound that consists of a cyclohexane ring with two amine groups attached to it, each containing a methanesulfonyl (CH3SO2) group. (1R,2R)-1,2-N,N'-BIS[(METHANE-SULFONYL)AMINO]-CYCLOHEXANE is a chiral molecule with a specific stereochemistry, denoted by the (1R,2R) prefix. It is used in organic synthesis and as a reagent in various chemical reactions, particularly in the formation of chiral compounds. The methanesulfonyl groups can act as protecting groups for amines, allowing for selective reactions in organic synthesis. Additionally, this compound may have potential applications in medicinal chemistry and pharmaceutical research due to its chiral nature and the presence of amine groups, which are common functionalities in biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 122833-58-3 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, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 122833-58:
(8*1)+(7*2)+(6*2)+(5*8)+(4*3)+(3*3)+(2*5)+(1*8)=113
113 % 10 = 3
So 122833-58-3 is a valid CAS Registry Number.

122833-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number	-
Other names	(1R,2R)-trans-1,2-bis(methylsulfonylamino)cyclohexane

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:122833-58-3 SDS

122833-58-3Upstream product

• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 124-63-0 methanesulfonyl chloride 

122833-58-3Downstream Products

122833-58-3Relevant articles and documents

Discovery of chiral cyclopropyl dihydro-alkylthio-benzyl-oxopyrimidine (5-DABO) derivatives as potent HIV-1 reverse transcriptase inhibitors with high activity against clinically relevant mutants

Radi, Marco,Maga, Giovanni,Alongi, Maddalena,Angeli, Lucilla,Samuele, Alberta,Zanoli, Samantha,Bellucci, Luca,Tafi, Andrea,Casaluce, Gianni,Giorgi, Gianluca,Armand-Ugon, Mercedes,Gonzalez, Emmanuel,Este, José A.,Baltzinger, Mireille,Bec, Guillaume,Dumas, Philippe,Ennifar, Eric,Botta, Maurizio

supporting information; experimental part, p. 840 - 851 (2009/12/26)

The role played by stereochemistry in the C2-substituent (left part) on the S-DABO scaffold for anti-HIV-1 activity has been investigated for the first time. A series of S-DABO analogues, where the double bond in the C2-substituent is replaced by an enant

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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