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102362-49-2

3,7,12-trihydroxy-7-methylcholanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102362-49-2 Structure

  • Basic information

    1. Product Name: 3,7,12-trihydroxy-7-methylcholanoic acid
    2. Synonyms: 3,7,12-trihydroxy-7-methylcholanoic acid
    3. CAS NO:102362-49-2
    4. Molecular Formula: C25H42 O5
    5. Molecular Weight: 422.6
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102362-49-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 583.6°Cat760mmHg
    3. Flash Point: 320.8°C
    4. Appearance: /
    5. Density: 1.163g/cm3
    6. Vapor Pressure: 4.74E-16mmHg at 25°C
    7. Refractive Index: 1.55
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 4.76±0.10(Predicted)
    11. CAS DataBase Reference: 3,7,12-trihydroxy-7-methylcholanoic acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3,7,12-trihydroxy-7-methylcholanoic acid(102362-49-2)
    13. EPA Substance Registry System: 3,7,12-trihydroxy-7-methylcholanoic acid(102362-49-2)

  • 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: 102362-49-2(Hazardous Substances Data)

102362-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102362-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,6 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102362-49:
(8*1)+(7*0)+(6*2)+(5*3)+(4*6)+(3*2)+(2*4)+(1*9)=82
82 % 10 = 2
So 102362-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H42O5/c1-14(5-8-21(28)29)17-6-7-18-22-19(12-20(27)25(17,18)4)23(2)10-9-16(26)11-15(23)13-24(22,3)30/h14-20,22,26-27,30H,5-13H2,1-4H3,(H,28,29)/t14-,15+,16-,17-,18+,19?,20+,22+,23+,24-,25-/m1/s1

102362-49-2Downstream Products

102362-49-2Relevant articles and documents

Synthesis and antitumor activity of alkylated bile acids and oxazolines

Bjedov, Sr?an,Jakimov, Dimitar,Po?a, Mihalj,Klisuri?, Olivera R.,Saka?, Marija

, p. 6932 - 6941 (2017)

Bile acid derivatives with a free carboxylic group or an oxazoline ring in the side chain and with different lengths of alkyl chains on steroid skeleton were synthetized and their antitumor activity against six human cancer cell lines was investigated. Methyl, ethyl, butyl or octyl chains were introduced stereoselectively by Grignard reaction at C-7 of acid and oxazoline, and at C-12 of oxazoline. Carbonyl group at C-12 of acid compound gave addition product only with methyl Grignard reagent, and complex mixture of products with other used reagents. Due to enolization, the C-3 carbonyl group did not participate in the Grignard reaction. Steric reasons are a main cause of this chemical behavior. Compounds with a butyl chain at the C-7 position showed very good antitumor activity with IC50 5 μM.

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