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CAS

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27894-82-2

p-nitrophenyl 1-thio-β-D-lactoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 27894-82-2 Structure

  • Basic information

    1. Product Name: p-nitrophenyl 1-thio-β-D-lactoside
    2. Synonyms: p-nitrophenyl 1-thio-β-D-lactoside
    3. CAS NO:27894-82-2
    4. Molecular Formula:
    5. Molecular Weight: 479.462
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27894-82-2.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-nitrophenyl 1-thio-β-D-lactoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: p-nitrophenyl 1-thio-β-D-lactoside(27894-82-2)
    11. EPA Substance Registry System: p-nitrophenyl 1-thio-β-D-lactoside(27894-82-2)

  • 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: 27894-82-2(Hazardous Substances Data)

27894-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27894-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27894-82:
(7*2)+(6*7)+(5*8)+(4*9)+(3*4)+(2*8)+(1*2)=162
162 % 10 = 2
So 27894-82-2 is a valid CAS Registry Number.

27894-82-2Relevant articles and documents

Aryl O- and S-galactosides and lactosides as specific inhibitors of human galectins-1 and -3: Role of electrostatic potential at O-3

Giguere, Denis,Sato, Sachiko,St-Pierre, Christian,Sirois, Suzanne,Roy, Rene

, p. 1668 - 1672 (2007/10/03)

Phase transfer catalyzed reaction was used for the high yielding synthesis of aryl 1-thio-β-d-galacto- and lacto-pyranosides carrying a panel of substituents on the phenyl groups. Best galectin-1 inhibitors were simple p-nitrophenyl thiogalactoside 5a for

Synthesis of glycopolymers containing GM3-saccharide

Cao,Roy

, p. 3421 - 3434 (2007/10/03)

GM3-trisaccharide [Neu5Acα-)2 → 3)-Galβ-(1 → 4)-Glcβ-(1 → OR] was synthesized using our 'active-latent' thioglycosylation strategy. The trisaccharide was prepared with a p-acrylamidophenyl aglycon for copolymerization with acrylamide. The resulting water-soluble sialyl α-(2 → 3)-lactoside copolyacrylamide with different carbohydrate incorporation was shown to possess antigenic properties.

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