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ethyl 2-benzamido-2-(4-bromophenylamino)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1330785-21-1 Structure
  • Basic information

    1. Product Name: ethyl 2-benzamido-2-(4-bromophenylamino)acetate
    2. Synonyms: ethyl 2-benzamido-2-(4-bromophenylamino)acetate
    3. CAS NO:1330785-21-1
    4. Molecular Formula:
    5. Molecular Weight: 377.238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1330785-21-1.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: ethyl 2-benzamido-2-(4-bromophenylamino)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-benzamido-2-(4-bromophenylamino)acetate(1330785-21-1)
    11. EPA Substance Registry System: ethyl 2-benzamido-2-(4-bromophenylamino)acetate(1330785-21-1)
  • 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: 1330785-21-1(Hazardous Substances Data)

1330785-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1330785-21-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,7,8 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1330785-21:
(9*1)+(8*3)+(7*3)+(6*0)+(5*7)+(4*8)+(3*5)+(2*2)+(1*1)=141
141 % 10 = 1
So 1330785-21-1 is a valid CAS Registry Number.

1330785-21-1Downstream Products

1330785-21-1Relevant articles and documents

A copper/O2-mediated direct sp3 C-H/N-H cross-dehydrogen coupling reaction of acylated amines and: N -aryl glycine esters

Sun, Bin,Wang, Yao,Li, Deyu,Jin, Can,Su, Weike

, p. 2902 - 2909 (2018)

A copper salt-catalyzed cross-dehydrogenative coupling reaction between N-aryl glycine esters and acylated amines has been developed. The reaction proceeded effectively under an oxygen atmosphere without the use of peroxide agents. This simple protocol al

Cu(II)-catalyzed intermolecular amidation of C-acylimine: A convenient access to gem-diamino acid derivatives

Zhu, Shujie,Dong, Jia,Fu, Shaomin,Jiang, Huanfeng,Zeng, Wei

, p. 4914 - 4917 (2011/11/06)

C-Acylimines 1 undergo intermolecular amidation with amides 2 to produce monoacyl gem-diamino acid derivatives 3 upon treatment with Cu(OTf)2 (20 mol %)/ PPh3 (20 mol %) under mild conditions. This method provides an efficient access to gem-diamino acid equivalents with good to excellent yields.

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