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1327165-96-7

C23H27ClO8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1327165-96-7 Structure

  • Basic information

    1. Product Name: C23H27ClO8
    2. Synonyms:
    3. CAS NO:1327165-96-7
    4. Molecular Formula:
    5. Molecular Weight: 466.916
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1327165-96-7.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: C23H27ClO8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H27ClO8(1327165-96-7)
    11. EPA Substance Registry System: C23H27ClO8(1327165-96-7)

  • 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: 1327165-96-7(Hazardous Substances Data)

1327165-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1327165-96-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,7,1,6 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1327165-96:
(9*1)+(8*3)+(7*2)+(6*7)+(5*1)+(4*6)+(3*5)+(2*9)+(1*6)=157
157 % 10 = 7
So 1327165-96-7 is a valid CAS Registry Number.

1327165-96-7Downstream Products

1327165-96-7Relevant articles and documents

C-Aryl glucosides substituted at the 4′-position as potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the treatment of type 2 diabetes

Xu, Baihua,Feng, Yan,Cheng, Huawei,Song, Yanli,Lv, Binhua,Wu, Yuelin,Wang, Congna,Li, Shengbin,Xu, Min,Du, Jiyan,Peng, Kun,Dong, Jiajia,Zhang, Wenbin,Zhang, Ting,Zhu, Liangcheng,Ding, Haifeng,Sheng, Zelin,Welihinda, Ajith,Roberge, Jacques Y.,Seed, Brian,Chen, Yuanwei

, p. 4465 - 4470 (2011)

A series of C-aryl glucosides with various substituents at the 4′-position of the distal aryl ring have been synthesized and evaluated for inhibition of hSGLT1 and hSGLT2. Introduction of alkyl or alkoxy substituents at the 4′-position was found to improve SGLT2 potency, whereas introduction of a hydrophilic group at this position was deleterious. Compounds with alkoxy-, cycloalkoxy- or cycloalkenyloxy-ethoxy scaffolds exhibited good inhibitory activity and high selectivity toward SGLT2. Selected compounds were investigated for in vivo efficacy.

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