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1057653-08-3

2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1057653-08-3 Structure

  • Basic information

    1. Product Name: 2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid
    2. Synonyms: 2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid
    3. CAS NO:1057653-08-3
    4. Molecular Formula:
    5. Molecular Weight: 295.746
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1057653-08-3.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: 2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid(1057653-08-3)
    11. EPA Substance Registry System: 2-{[(5-chlorothiophen-2-yl)carbonyl]aminomethyl}benzoic acid(1057653-08-3)

  • 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: 1057653-08-3(Hazardous Substances Data)

1057653-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1057653-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,7,6,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1057653-08:
(9*1)+(8*0)+(7*5)+(6*7)+(5*6)+(4*5)+(3*3)+(2*0)+(1*8)=153
153 % 10 = 3
So 1057653-08-3 is a valid CAS Registry Number.

1057653-08-3Relevant articles and documents

2-Aminomethylphenylamine as a novel scaffold for factor Xa inhibitor

Mochizuki, Akiyoshi,Nagata, Tsutomu,Kanno, Hideyuki,Suzuki, Makoto,Ohta, Toshiharu

experimental part, p. 1623 - 1642 (2011/04/21)

We have been researching orally active factor Xa inhibitor for a long time. We explored the new diamine linker using effective ligands to obtain a new attractive original scaffold 2-aminomethylphenylamine derivative. Compound 1D showed very strong in vitro and in vivo factor Xa inhibitory activity, as well as favorable PK profiles in po administration to monkeys.

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