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1006037-04-2

Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1006037-04-2 Structure

  • Basic information

    1. Product Name: Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1)
    2. Synonyms: Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1);UTNGQFGMAUMZED-UHFFFAOYSA-N
    3. CAS NO:1006037-04-2
    4. Molecular Formula: CH4O3S*C11H13NO2
    5. Molecular Weight: 287.33208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1006037-04-2.mol

  • 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: Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1)(1006037-04-2)
    11. EPA Substance Registry System: Benzoic acid, 4-(1-aminocyclopropyl)-, methyl ester, methanesulfonate (1:1)(1006037-04-2)

  • 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: 1006037-04-2(Hazardous Substances Data)

1006037-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1006037-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,0,3 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1006037-04:
(9*1)+(8*0)+(7*0)+(6*6)+(5*0)+(4*3)+(3*7)+(2*0)+(1*4)=82
82 % 10 = 2
So 1006037-04-2 is a valid CAS Registry Number.

1006037-04-2Relevant articles and documents

Scalable synthesis of a prostaglandin EP4 receptor antagonist

Gauvreau, Danny,Dolman, Sarah J.,Hughes, Greg,Oshea, Paul D.,Davies, Ian W.

supporting information; experimental part, p. 4078 - 4085 (2010/08/22)

The evolution of scalable, economically viable synthetic approaches to the potent and selective prostaglandin EP4 antagonist 1 is presented. The chromatography-free synthesis of multikilogram quantities of 1 using a seven-step sequence (six in the longest

PROCESS FOR MAKING INDOLE CYCLOPROPYL AMIDE DERIVATIVES

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Page/Page column 9; 14, (2010/11/05)

An efficient and economical process for synthesizing kilogram quantities of an indole cyclopropyl amide derivative of Formula (I), or a pharmaceutically acceptable salt thereof, is disclosed. The process comprises the coupling of indolecarboxylic acid der

PROCESS FOR MAKING THIOPHENE CARBOXAMIDE DERIVATIVE

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Page/Page column 13-15, (2009/04/25)

The invention encompasses a process for making a thiophene carboxamide derivative, which is an EP4 antagonist useful for treating pain and inflammation.

THIOPHENECARBOXAMIDE DERIVATIVES AS EP4 RECEPTOR LIGANDS

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Page/Page column 71, (2008/06/13)

The invention is directed to thiophenecarboxamide derivatives of formulae I and II as EP4 receptor ligands, antagonists or agonists, useful for the treatment of EP4 mediated diseases or conditions, such as acute and chronic pain, osteoarthritis, rheumatoi

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