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CAS

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157029-52-2

methyl (methyl 2-O-benzyl-5-deoxy-5-trifluoroacetamido-α-D-galactofuranosid)uronate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 157029-52-2 Structure

  • Basic information

    1. Product Name: methyl (methyl 2-O-benzyl-5-deoxy-5-trifluoroacetamido-α-D-galactofuranosid)uronate
    2. Synonyms:
    3. CAS NO:157029-52-2
    4. Molecular Formula:
    5. Molecular Weight: 407.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 157029-52-2.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: methyl (methyl 2-O-benzyl-5-deoxy-5-trifluoroacetamido-α-D-galactofuranosid)uronate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (methyl 2-O-benzyl-5-deoxy-5-trifluoroacetamido-α-D-galactofuranosid)uronate(157029-52-2)
    11. EPA Substance Registry System: methyl (methyl 2-O-benzyl-5-deoxy-5-trifluoroacetamido-α-D-galactofuranosid)uronate(157029-52-2)

  • 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: 157029-52-2(Hazardous Substances Data)

157029-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 157029-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,0,2 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157029-52:
(8*1)+(7*5)+(6*7)+(5*0)+(4*2)+(3*9)+(2*5)+(1*2)=132
132 % 10 = 2
So 157029-52-2 is a valid CAS Registry Number.

157029-52-2Upstream product

157029-52-2Relevant articles and documents

Synthesis of (+)-Galactostatin and (+)-1-Deoxygalactostatin utilizing L-Quebrachitol as a Chiral Building Block

Chida, Noritaka,Tanikawa, Tetsuya,Tobe, Takahiko,Ogawa, Seiichiro

, p. 1247 - 1248 (1994)

The stereoselective conversion of the naturally occurring optically active cyclitol, L-quebrachitol 1, into galactosidase inhibitors, (+)-galactostatin 2 and (+)-1-deoxygalactostatin 3 is described; the key steps in this synthesis are (i) stereoselective

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