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CAS

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871714-03-3

Carbamic acid, [[5-[(2-chlorophenyl)methyl]-2-thienyl]methyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 871714-03-3 Structure

  • Basic information

    1. Product Name: Carbamic acid, [[5-[(2-chlorophenyl)methyl]-2-thienyl]methyl]-, 1,1-dimethylethyl ester
    2. Synonyms:
    3. CAS NO:871714-03-3
    4. Molecular Formula: C17H20ClNO2S
    5. Molecular Weight: 337.87
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871714-03-3.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: Carbamic acid, [[5-[(2-chlorophenyl)methyl]-2-thienyl]methyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [[5-[(2-chlorophenyl)methyl]-2-thienyl]methyl]-, 1,1-dimethylethyl ester(871714-03-3)
    11. EPA Substance Registry System: Carbamic acid, [[5-[(2-chlorophenyl)methyl]-2-thienyl]methyl]-, 1,1-dimethylethyl ester(871714-03-3)

  • 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: 871714-03-3(Hazardous Substances Data)

871714-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 871714-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,7,1 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 871714-03:
(8*8)+(7*7)+(6*1)+(5*7)+(4*1)+(3*4)+(2*0)+(1*3)=173
173 % 10 = 3
So 871714-03-3 is a valid CAS Registry Number.

871714-03-3Relevant articles and documents

Structure and activity relationships of tartrate-based TACE inhibitors

Li, Dansu,Popovici-Muller, Janeta,Belanger, David B.,Caldwell, John,Dai, Chaoyang,David, Maria,Girijavallabhan, Vinay M.,Lavey, Brian J.,Lee, Joe F.,Liu, Zhidan,Mazzola, Rob,Rizvi, Razia,Rosner, Kristin E.,Shankar, Bandarpalle,Spitler, Jim,Ting, Pauline C.,Vaccaro, Henry,Yu, Wensheng,Zhou, Guowei,Zhu, Zhaoning,Niu, Xiaoda,Sun, Jing,Guo, Zhuyan,Orth, Peter,Chen, Shiying,Kozlowski, Joseph A.,Lundell, Daniel J.,Madison, Vincent,McKittrick, Brian,Piwinski, John J.,Shih, Neng-Yang,Shipps Jr., Gerald W.,Siddiqui, M. Arshad,Strickland, Corey O.

scheme or table, p. 4812 - 4815 (2010/10/02)

The syntheses and structure-activity relationships of the tartrate-based TACE inhibitors are discussed. The optimization of both the prime and non-prime sites led to compounds with picomolar activity. Several analogs demonstrated good rat pharmacokinetics

COMPOUNDS FOR THE TREATMENT OF INFLAMMATORY DISORDERS

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Page/Page column 361, (2010/02/15)

This invention relates to compounds of the Formula (I) or a pharmaceutically acceptable salt, solvate or isomer thereof, which can be useful for the treatment of diseases or conditions mediated by MMPs, ADAMs, TACE, TNF-α or combinations thereof.

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