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1036750-30-7

C18H17ClN2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036750-30-7 Structure

  • Basic information

    1. Product Name: C18H17ClN2O2
    2. Synonyms: C18H17ClN2O2
    3. CAS NO:1036750-30-7
    4. Molecular Formula:
    5. Molecular Weight: 328.798
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036750-30-7.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: C18H17ClN2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H17ClN2O2(1036750-30-7)
    11. EPA Substance Registry System: C18H17ClN2O2(1036750-30-7)

  • 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: 1036750-30-7(Hazardous Substances Data)

1036750-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036750-30-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1036750-30:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*5)+(3*0)+(2*3)+(1*0)=127
127 % 10 = 7
So 1036750-30-7 is a valid CAS Registry Number.

1036750-30-7Downstream Products

1036750-30-7Relevant articles and documents

Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a

Onda, Kenichi,Suzuki, Takayuki,Shiraki, Ryota,Yonetoku, Yasuhiro,Negoro, Kenji,Momose, Kazuhiro,Katayama, Naoko,Orita, Masaya,Yamaguchi, Tomohiko,Ohta, Mitsuaki,Tsukamoto, Shin-ichi

, p. 5452 - 5464 (2008/12/21)

A series of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives were prepared and evaluated as inhibitors of human liver glycogen phosphorylase a (hLGPa). One compound, 5-chloro-N-[4-(1,2-dihydroxyethyl)phenyl]-1H-indole-2-carboxamide (2f), inhibited hLGPa with an IC50 of 0.90 μM. The pyridine analogue of 2f showed inhibitory activity of glucagon-induced glucose output in cultured primary hepatocytes with an IC50 of 0.62 μM and oral hypoglycemic activity in diabetic db/db mice. Crystallographic determination of the complex of 2f with hLGPa showed binding of the inhibitor in a solvent cavity at the dimer interface, with the two hydroxyl groups making favorable electrostatic interactions with hLGPa.

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