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(1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 894493-95-9 Structure
  • Basic information

    1. Product Name: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine
    2. Synonyms: (1S,2S)-(+)-N,N-Dimethyl diaminocyclohexane;(1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine;(1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine;(1S,2S)-N,N-Dimethyl-1,2-cyclohexanediamine;1R,2R-(-)-OR1S,2S-(+)-N,N-DIAMINOCYCLOHEXANE;N,N'-Dimethyl-1S,2S-Diaminocyclohexane;(1S,2S)-1-N,1-N-diMethylcyclohexane-1,2-diaMine;1S,2S-(+)-N,N-diaminocyclohexane
    3. CAS NO:894493-95-9
    4. Molecular Formula: C8H18N2
    5. Molecular Weight: 142.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 894493-95-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 180 °C
    3. Flash Point: 62 °C
    4. Appearance: /
    5. Density: 0.92
    6. Refractive Index: 1.49
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. PKA: 10.52±0.70(Predicted)
    10. CAS DataBase Reference: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(CAS DataBase Reference)
    11. NIST Chemistry Reference: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(894493-95-9)
    12. EPA Substance Registry System: (1S,2S)-(+)-N,N-Dimethylcyclohexane-1,2-diamine(894493-95-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 22-34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: 2735
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 8
    8. PackingGroup:
    9. Hazardous Substances Data: 894493-95-9(Hazardous Substances Data)

894493-95-9 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 894493-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,4,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 894493-95:
(8*8)+(7*9)+(6*4)+(5*4)+(4*9)+(3*3)+(2*9)+(1*5)=239
239 % 10 = 9
So 894493-95-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N2/c1-10(2)8-6-4-3-5-7(8)9/h7-8H,3-6,9H2,1-2H3/t7-,8-/m0/s1

894493-95-9SDS

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 (1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine

1.2 Other means of identification

Product number -
Other names (1S,2S)-2-N,2-N-dimethylcyclohexane-1,2-diamine

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:894493-95-9 SDS

894493-95-9Relevant articles and documents

Preparation of C 2-Symmetric Biaryl Bisiminium Salts and Their Use as Organocatalysts for Asymmetric Epoxidation

Bulman Page, Philip C.,Farah, Mohamed M.,Buckley, Benjamin R.,Chan, Yohan,Blacker, A. John

supporting information, p. 126 - 130 (2015/12/26)

Two C 2-symmetric bisiminium salt species containing biphenylazepinium units and derived from two chiral diamines were prepared and tested as organocatalysts for asymmetric epoxidation.

Stereoselective reaction of 2-carboxythioesters-1,3-dithiane with nitroalkenes: An organocatalytic strategy for the asymmetric addition of a glyoxylate anion equivalent

Massolo, Elisabetta,Benaglia, Maurizio,Genoni, Andrea,Annunziata, Rita,Celentano, Giuseppe,Gaggero, Nicoletta

supporting information, p. 5591 - 5596 (2015/05/27)

An efficient organocatalytic methodology has been developed to perform the stereoselective addition of 2-carboxythioesters-1,3-dithiane to nitroalkenes. Under mild reaction conditions γ-nitro-β-aryl-α-keto esters with up to 92% ee were obtained, realizing a formal catalytic stereoselective conjugate addition of the glyoxylate anion synthon. The reaction products are versatile starting materials for further synthetic transformations; for example, the simultaneous reduction of the nitro group and removal of the dithiane ring was accomplished, allowing the preparation of a GABAB receptor agonist baclofen.

Asymmetric isomerization of ω-hydroxy-α,β-unsaturated thioesters into β-mercaptolactones by a bifunctional aminothiourea catalyst

Fukata, Yukihiro,Okamura, Takaaki,Asano, Keisuke,Matsubara, Seijiro

supporting information, p. 2184 - 2187 (2014/05/06)

We present a novel methodology for the asymmetric synthesis of β-mercaptolactones via isomerization of ω-hydroxy-α,β- unsaturated thioesters by means of a bifunctional aminothiourea catalyst. The catalyst interacts with the substrate through the cooperati

Asymmetric Michael addition of arylthiols to α,β-unsaturated carbonyl compounds catalyzed by bifunctional organocatalysts

Li, Bang-Jing,Jiang, Lin,Liu, Min,Chen, Ying-Chun,Ding, Li-Sheng,Wu, Yong

, p. 603 - 606 (2007/10/03)

Bifunctional chiral organocatalysts comprising thiourea and tertiary amine groups were synthesized. They act as efficient catalysts for asymmetric Michael addition of arylthiols to α,β-unsaturated carbonyl compounds. Enantioselectivity up to 85% has been achieved. Asymmetric α-protonation reaction (up to 60% ee) can be obtained in the presence of the bifunctional catalyst.

Analgesic N-[2-(furyl-methylamino and 2-thienylmethylamino)cycloaliphatic]be

-

, (2008/06/13)

Cis - and trans-N-(2-aminocycycloaliphatic)benzamide compounds of the formula STR1 e.g., N-methyl-N-[2-[(2-furylmethyl)methylamino]-cyclohexyl]-3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm-blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.

Analgesic N-{2-[N'-(2-furylmethyl and 2-thienyl-methyl)-N'-alkylamino]cycloaliphatic}cyanobenzamides

-

, (2008/06/13)

Cis- and trans-N-(2-aminocycloaliphatic)benzamide compounds of the formula STR1 e.g., N-methyl-N-[2-(N-pyrrolidinyl)cyclohexyl]-3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.

Analgesic N-(2-aminocycloaliphatic)benzamides

-

, (2008/06/13)

Cis- and trans-N-(2-aminocycloaliphatic)benzamide compounds of the formula STR1 E.G., N-methyl-N[2-(N-pyrrolidinyl)cyclohexyl[3,4-dichlorobenzamide, and their pharmaceutically acceptable salts, have been found to have potent analgesic activity, and compositions containing these compounds useful in pharmaceutical dosage unit form for alleviating pain in warm blooded animals, as well as methods for alleviating pain in animals with these compositions. Processes for preparing the compounds are also disclosed.

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