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124676-22-8

N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124676-22-8 Structure

  • Basic information

    1. Product Name: N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide
    2. Synonyms: N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide
    3. CAS NO:124676-22-8
    4. Molecular Formula:
    5. Molecular Weight: 250.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124676-22-8.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: N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide(124676-22-8)
    11. EPA Substance Registry System: N-{[(Amino-carbamoyl-methyl)-carbamoyl]-methyl}-benzamide(124676-22-8)

  • 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: 124676-22-8(Hazardous Substances Data)

124676-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124676-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,7 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124676-22:
(8*1)+(7*2)+(6*4)+(5*6)+(4*7)+(3*6)+(2*2)+(1*2)=128
128 % 10 = 8
So 124676-22-8 is a valid CAS Registry Number.

124676-22-8Downstream Products

124676-22-8Relevant articles and documents

Benzotriazole-assisted Synthesis of Monoacyl α-Aminoglycines

Katritzky, Alan R.,Urogdi, Laszlo,Mayence, Annie

, p. 337 - 338 (1989)

Adducts (8,12) derived from benzotriazole (7), glyoxylic ester (6) or acid (11), and an amide (5), react with ammonia in a novel, convenient route to monoacylated α-aminoglycines (9,13) useful for the synthesis of peptide analogues.

Benzotriazole-Assisted Synthesis of Monoacyl Aminals and Their Peptide Derivatives

Katritzky, Alan R.,Urogdi, Laszlo,Mayence, Annie

, p. 2206 - 2214 (2007/10/02)

Adducts 8-11, derived from benzotriazole (7), an aldehyde (6), and an amide (5), react with ammonia to give various monoacylated aminals (12-14) and "gem-peptide" derivatives (15) in a novel, convenient route, useful for peptide analogue syntheses and stu

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