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  • 101-12-2 Structure
  • Basic information

    1. Product Name: 3,3'-Diaminobenzanilide
    2. Synonyms: 3,3'-diaminobenzanilide;3-aminophenyl 3-aminobenzoate;N-(3-Aminophenyl)-3-aminobenzamide;3-azanyl-N-(3-azanylphenyl)benzamide
    3. CAS NO:101-12-2
    4. Molecular Formula: C13H13N3O
    5. Molecular Weight: 227.26182
    6. EINECS: 202-917-3
    7. Product Categories: N/A
    8. Mol File: 101-12-2.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,3'-Diaminobenzanilide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3'-Diaminobenzanilide(101-12-2)
    11. EPA Substance Registry System: 3,3'-Diaminobenzanilide(101-12-2)
  • 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: 101-12-2(Hazardous Substances Data)

101-12-2 Usage

Description

3,3'-Diaminobenzanilide is a chemical compound characterized by its molecular structure that includes two amino groups (-NH2) bonded to a central benzene ring, which is additionally substituted with an anilide group. 3,3'-diaminobenzanilide is pivotal in organic synthesis, especially for the creation of aromatic compounds, dyes, and pharmaceuticals. Its utility stems from its capacity to act as a fundamental building block in the synthesis of more intricate organic molecules.

Uses

Used in Organic Synthesis:
3,3'-Diaminobenzanilide is used as a key intermediate for the synthesis of various aromatic compounds due to its reactive amino and anilide groups, which facilitate the formation of a wide range of organic molecules.
Used in Pharmaceutical Industry:
3,3'-Diaminobenzanilide is utilized as a building block in the development of pharmaceuticals, leveraging its chemical reactivity to create new drug candidates with potential therapeutic applications.
Used in Dye Manufacturing:
In the dye industry, 3,3'-Diaminobenzanilide is employed as a precursor for the production of dyes, capitalizing on its molecular structure to yield dyes with specific color properties and stability.
Each application takes advantage of the unique structural features of 3,3'-diaminobenzanilide, highlighting its multifaceted role in different sectors of the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 101-12-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101-12:
(5*1)+(4*0)+(3*1)+(2*1)+(1*2)=12
12 % 10 = 2
So 101-12-2 is a valid CAS Registry Number.

101-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-N-(3-aminophenyl)benzamide

1.2 Other means of identification

Product number -
Other names 3,3'-Diaminobenzanilid

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:101-12-2 SDS

101-12-2Relevant articles and documents

Naphthalene-1,8-diylbis(diphenylmethylium) as an organic two-electron oxidant: Benzidine synthesis via oxidative self-coupling of N,N-dialkylanilines

Saitoh, Terunobu,Yoshida, Suguru,Ichikawa, Junji

, p. 6414 - 6419 (2007/10/03)

Naphthalene-1,8-diylbis(diphenylmethylium) exhibits a unique electron-transfer reduction behavior due to the close proximity of the two triarylmethyl cations, which form a C-C bond while accepting two electrons, leading to 1,1,2,2-tetraphenylacenaphthene. The preparation of the dication was readily accomplished under anhydrous conditions starting from a cyclic bis(triarylmethyl) ether, derived from 1,8-dibromonaphthalene. The process proceeded via deoxygenation accompanying the formation of a disiloxane on treatment with a silylating agent (Me3SiClO4 or Me 3SiOTf) in 1,1,1,3,3,3-hexafluoropropan-2-ol. The dication was successfully employed for oxidative coupling of N,N-dialkylanilines at the paraposition to afford the corresponding benzidines in good to excellent yield.

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