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637029-19-7

(22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 637029-19-7 Structure

  • Basic information

    1. Product Name: (22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten
    2. Synonyms: (22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten
    3. CAS NO:637029-19-7
    4. Molecular Formula:
    5. Molecular Weight: 536.795
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 637029-19-7.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: (22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten(CAS DataBase Reference)
    10. NIST Chemistry Reference: (22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten(637029-19-7)
    11. EPA Substance Registry System: (22R,25R)-3β-hydroxy-26-p-methoxybenzyloxy-5-furosten(637029-19-7)

  • 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: 637029-19-7(Hazardous Substances Data)

637029-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 637029-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,0,2 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 637029-19:
(8*6)+(7*3)+(6*7)+(5*0)+(4*2)+(3*9)+(2*1)+(1*9)=157
157 % 10 = 7
So 637029-19-7 is a valid CAS Registry Number.

637029-19-7Relevant articles and documents

Synthesis of Dihydrodiosgenin Glycosides as Mimetics of Bidesmosidic Steroidal Saponins

Suhr, Rene,Lahmann, Martina,Oscarson, Stefan,Thiem, Joachim

, p. 4003 - 4011 (2007/10/03)

The focus of this work is the synthesis of bidesmosidic saponin mimetics. Therefore, dihydrodiosgenin derivatives, which differ from the natural compounds by reduction of the 22-(hemi) acetal were used as glycosyl acceptors. In preliminary studies, the dihydrodiosgenin glycosides 16, 17 and 19, as well as trisaccharide 22, were synthesized. The acceptors 10 and 14 were subjected to DMTST-mediated glucosylation for the synthesis of the chacotriose-substituted compound 3. For a selective 2,4-di-rhamnosylation of the dihydrodiosgenin glucopyranoside, differentiation of the glucose OH groups was achieved by selective benzoylation with 1-(benzoyloxy)benzotriazole. Reaction of the 3,6-di-O-benzoate 32 with the perbenzoylated ethyl thiorhamnopyranoside donor 15 gave the 2,4-di-rhamnosylated compound 33, together with the mono-rhamnosylated derivative. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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