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5-chloro-1H-benzoimidazole-2-sulfonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 251921-01-4 Structure
  • Basic information

    1. Product Name: 5-chloro-1H-benzoimidazole-2-sulfonyl chloride
    2. Synonyms:
    3. CAS NO:251921-01-4
    4. Molecular Formula:
    5. Molecular Weight: 251.093
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 251921-01-4.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: 5-chloro-1H-benzoimidazole-2-sulfonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-chloro-1H-benzoimidazole-2-sulfonyl chloride(251921-01-4)
    11. EPA Substance Registry System: 5-chloro-1H-benzoimidazole-2-sulfonyl chloride(251921-01-4)
  • 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: 251921-01-4(Hazardous Substances Data)

251921-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251921-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,9,2 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 251921-01:
(8*2)+(7*5)+(6*1)+(5*9)+(4*2)+(3*1)+(2*0)+(1*1)=114
114 % 10 = 4
So 251921-01-4 is a valid CAS Registry Number.

251921-01-4Downstream Products

251921-01-4Relevant articles and documents

Design, synthesis, and biological activity of non-basic compounds as factor Xa inhibitors: SAR study of S1 and aryl binding sites

Komoriya, Satoshi,Haginoya, Noriyasu,Kobayashi, Shozo,Nagata, Tsutomu,Mochizuki, Akiyoshi,Suzuki, Masanori,Yoshino, Toshiharu,Horino, Haruhiko,Nagahara, Takayasu,Suzuki, Makoto,Isobe, Yumiko,Furugoori, Taketoshi

, p. 3927 - 3954 (2007/10/03)

Compound 7 was identified as the active metabolite of 6 by HPLC and mass spectral analysis. Modification of lead compound 7 by transformation of its N-oxide 6-6 biaryl ring system and fused aromatics produced a series of non-basic fXa inhibitors with excellent potency in anti-fXa and anticoagulant assays. The optimized compounds 73b and 75b showed sub to one digit micromolar anticoagulant activity (PTCT2). Particularly, anti-fXa activity was detected in plasma of rats orally administered with 1 mg/kg of compound 75b.

Sulfonic acid sulfonylamino n-(heteroaralkyl)-azaheterocyclylamide compounds

-

, (2008/06/13)

The compounds of formula I herein exhibit useful pharmacological activity and accordingly are incorporated into pharmaceutical compositions and used in the treatment of patients suffering from certain medical disorders. More specifically, they are inhibitors of the activity of Factor Xa. The present invention is directed to compounds of formula I, compositions containing compounds of formula I, and their use, for treating a patient suffering from, or subject to, a physiological condition which can be ameliorated by the administration of an inhibitor of the activity of Factor Xa.

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