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CAS

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83600-07-1

1-nitro-2-phenylaminoethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83600-07-1 Structure

  • Basic information

    1. Product Name: 1-nitro-2-phenylaminoethane
    2. Synonyms: 1-nitro-2-phenylaminoethane
    3. CAS NO:83600-07-1
    4. Molecular Formula:
    5. Molecular Weight: 166.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83600-07-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-nitro-2-phenylaminoethane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-nitro-2-phenylaminoethane(83600-07-1)
    11. EPA Substance Registry System: 1-nitro-2-phenylaminoethane(83600-07-1)

  • 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: 83600-07-1(Hazardous Substances Data)

83600-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83600-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,0 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83600-07:
(7*8)+(6*3)+(5*6)+(4*0)+(3*0)+(2*0)+(1*7)=111
111 % 10 = 1
So 83600-07-1 is a valid CAS Registry Number.

83600-07-1Relevant articles and documents

Organocatalytic enantioselective formal C(sp2)-H alkylation

Manna, Madhu Sudan,Mukherjee, Santanu

supporting information, p. 130 - 133 (2015/01/30)

An organocatalytic enantioselective formal C(sp2)-H alkylation is reported. This alkylative desymmetrization of prochiral 2,2-disubstituted cyclopentene-1,3-dione is catalyzed by a bifunctional tertiary aminourea derivative, utilizes air-stable and inexpensive nitroalkanes as the alkylating agents, and delivers synthetically versatile five-membered carbocycles containing an all-carbon quaternary stereogenic center remote from the reaction site in excellent enantioselectivity.

Synthesis of some 2-aminonitroethanes via silica gel-catalyzed nitro-Mannich reaction

Mahasneh, Ali S.

, p. 1162 - 1165 (2008/09/18)

A direct one pot, three-component nitro-Mannich reaction of a nonenolizable aldehyde, aniline or one of its ring-substituted derivatives and nitromethane was carried out on silica gel surface. The products of the reaction, 2-aminonitroethane, were obtaine

NITROEHYLENE: NITROETHYLATON OF AMINES

Ranganathan, D.,Ranganathan, S.,Bamezai, S.

, p. 2789 - 2792 (2007/10/02)

The nitroehylation of amines is demosntrated to be a general reaction for bases in the pKa range of 2 - 8 and that it proceeds through a key intra-molecular quenching step.The reaction, illustrated with aromatic amines, aliphatic amines and het

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