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methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 651302-41-9 Structure
  • Basic information

    1. Product Name: methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside
    2. Synonyms: methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside
    3. CAS NO:651302-41-9
    4. Molecular Formula:
    5. Molecular Weight: 314.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 651302-41-9.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: methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside(651302-41-9)
    11. EPA Substance Registry System: methyl 3,4-dideoxy-6-O-tosyl-α-D-erythro-hex-3-enopyranoside(651302-41-9)
  • 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: 651302-41-9(Hazardous Substances Data)

651302-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651302-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,3,0 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 651302-41:
(8*6)+(7*5)+(6*1)+(5*3)+(4*0)+(3*2)+(2*4)+(1*1)=119
119 % 10 = 9
So 651302-41-9 is a valid CAS Registry Number.

651302-41-9Relevant articles and documents

Facile synthesis of 5-hydroxy-l-lysine from d-galactose as a chiral-precursor

Guo, Lina,Liu, Taibao,Chen, Kai,Song, Tianbang,Wang, Peng George,Zhao, Wei

, p. 7310 - 7317 (2014)

A concise synthesis of (2S,5R) and (2S,5S)-5-hydroxy-lysine was achieved by utilizing d-galactose as a chiral-precursor with stereo retention. This synthetic strategy showcased the potential of utilizing carbohydrates as starting materials to prepare amino acids. Using the diazido intermediate, the derived β-d-galactopyranosyl and α-d-glucopyranosyl-(1→2)- β-d-galactosyl moieties were synthesized. This journal is the Partner Organisations 2014.

Synthesis of Unsaturated Aminopyranosides as Possible Transition State Mimics for Glycosidases

Jordan, Allan M.,Osborn, Helen M. I.,Stafford, Petra M.,Tzortzis, George,Rastall, Robert A.

, p. 705 - 717 (2007/10/03)

Four unsaturated aminopyranosides have been prepared as possible transition-state mimics targeted towards carbohydrate processing enzymes. The conformations of the protonated aminosugars have been investigated by molecular modelling and their ability to i

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