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benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester

    Cas No: 306726-32-9

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  • SuZhou Yacoo Science Co., Ltd
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  • benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester

    Cas No: 306726-32-9

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  • 306726-32-9 Structure
  • Basic information

    1. Product Name: benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester
    2. Synonyms: benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester
    3. CAS NO:306726-32-9
    4. Molecular Formula:
    5. Molecular Weight: 1286.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 306726-32-9.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: benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester(306726-32-9)
    11. EPA Substance Registry System: benzoic acid 3-benzyloxy-2-(4-benzyloxy-3-methoxy-6-methoxymethyl-5-triisopropylsilanyloxy-tetrahydro-pyran-2-yloxy)-5-[4-(tert-butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-3-phenylselanyl-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-4-yl ester(306726-32-9)
  • 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: 306726-32-9(Hazardous Substances Data)

306726-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 306726-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,7,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 306726-32:
(8*3)+(7*0)+(6*6)+(5*7)+(4*2)+(3*6)+(2*3)+(1*2)=129
129 % 10 = 9
So 306726-32-9 is a valid CAS Registry Number.

306726-32-9Upstream product

306726-32-9Relevant articles and documents

Total synthesis of everninomicin 13,384-1 - Part 2: Synthesis of the FGHA2 fragment

Nicolaou,Mitchell, Helen J.,Fylaktakidou, Konstantina C.,Rodriguez, Rosa Maria,Suzuki, Hideo

, p. 3116 - 3148 (2007/10/03)

The stereoselective synthesis of everninomicin's 13,384-1 (1) FGHA2 fragment (2) in a suitable form for incorporation into the final target (1) is described. The construction of the FG 1,1′-disaccharide linkage relied on a new method based on tin-acetal chemistry, while for the GH orthoester bridge, a number of approaches were explored. Final success for the latter construction came when a novel 1,2-phenylseleno migration reaction was applied to couple rings G and H, followed by ketene acetal and orthoester formation.

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