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CAS

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157430-13-2

p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157430-13-2 Structure

  • Basic information

    1. Product Name: p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside
    2. Synonyms: p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside
    3. CAS NO:157430-13-2
    4. Molecular Formula:
    5. Molecular Weight: 236.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157430-13-2.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: p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside(157430-13-2)
    11. EPA Substance Registry System: p-methoxyphenyl 2,3,6-trideoxy-α-L-erythro-hex-2-enepyranoside(157430-13-2)

  • 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: 157430-13-2(Hazardous Substances Data)

157430-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157430-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,4,3 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 157430-13:
(8*1)+(7*5)+(6*7)+(5*4)+(4*3)+(3*0)+(2*1)+(1*3)=122
122 % 10 = 2
So 157430-13-2 is a valid CAS Registry Number.

157430-13-2Relevant articles and documents

Phenolic ferrier reaction and its application to the natural product synthesis

Noshita, Toshiro,Sugiyama, Takeyoshi,Kitazumi, Yoshiharu,Oritani, Takayuki

, p. 8259 - 8262 (1994)

Ferrier reaction between acetylglycals and phenols proceeded smoothly to give α-O-Δ2 glycosides predominantly. The products were converted to bio-active natural products.

Reagent Controlled Direct Dehydrative Glycosylation with 2-Deoxy Sugars: Construction of the Saquayamycin Z Pentasaccharide

Mizia, J. Colin,Bennett, Clay S.

, p. 5922 - 5927 (2019/08/27)

The first synthesis of the pentasaccharide fragment of the angucycline antibiotic saquayamycin Z is described. By using our sulfonyl chloride mediated reagent controlled dehydrative glycosylation, we are able to assemble the glycosidic linkages with high

Mitsunobu reactions of glycals with phenoxide nucleophiles are S(N)2'-selective

Sobti,Sulikowski

, p. 3661 - 3664 (2007/10/02)

The C3-hydroxyl group of L-rhamnal (4) and D-glucal 7 underwent S(N)2'-selective Mitsunobu displacements with substituted phenoxide nucleophiles. These reactions provide access to the corresponding α-arylglycoside.

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