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4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373921-68-6 Structure
  • Basic information

    1. Product Name: 4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside
    2. Synonyms: 4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside
    3. CAS NO:1373921-68-6
    4. Molecular Formula:
    5. Molecular Weight: 609.538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373921-68-6.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: 4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside(1373921-68-6)
    11. EPA Substance Registry System: 4-nitrophenyl β-D-fucopyranosyl-(1→4)-β-D-cellobioside(1373921-68-6)
  • 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: 1373921-68-6(Hazardous Substances Data)

1373921-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373921-68-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,9,2 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1373921-68:
(9*1)+(8*3)+(7*7)+(6*3)+(5*9)+(4*2)+(3*1)+(2*6)+(1*8)=176
176 % 10 = 6
So 1373921-68-6 is a valid CAS Registry Number.

1373921-68-6Downstream Products

1373921-68-6Relevant articles and documents

Glycosynthase with broad substrate specificity-an efficient biocatalyst for the construction of oligosaccharide library

Wei, Jinhua,Lv, Xun,Lue, Yang,Yang, Gangzhu,Fu, Lifeng,Yang, Liu,Wang, Jianjun,Gao, Jianhui,Cheng, Shuihong,Duan, Qian,Jin, Cheng,Li, Xuebing

, p. 2414 - 2419 (2013/05/23)

A versatile glycosynthase (TnG-E338A) with strikingly broad substrate scope has been developed from Thermus nonproteolyticus β-glycosidase (TnG) by using site-directed mutagenesis. The practical utility of this biocatalyst has been demonstrated by the facile generation of a small library containing various oligosaccharides and a steroidal glycoside (total 25 compounds) in up to 100 % isolated yield. Moreover, an array of eight gluco-oligosaccharides has been readily synthesized by the enzyme in a one-pot, parallel reaction, which highlights its potential in the combinatorial construction of a carbohydrate library that will assist glycomic and glycotherapeutic research. Significantly, the enzyme provides a means by which glycosynthase technology may be extended to combinatorial chemistry.

Rice BGlu1 glycosynthase and wild type transglycosylation activities distinguished by cyclophellitol inhibition

Pengthaisong, Salila,Chen, Chi-Fan,Withers, Stephen G.,Kuaprasert, Buabarn,Ketudat Cairns, James R.

experimental part, p. 51 - 59 (2012/05/04)

The rice BGlu1 β-d-glucosidase nucleophile mutant E386G is a glycosynthase that catalyzes the synthesis of cellooligosaccharides from α-d-glucopyranosyl fluoride (GlcF) donor and p-nitrophenyl (pNP) cellobioside (Glc2-pNP) or cello-oligosaccharide accepto

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