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C43H53NO19 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 874905-04-1 Structure
  • Basic information

    1. Product Name: C43H53NO19
    2. Synonyms: C43H53NO19
    3. CAS NO:874905-04-1
    4. Molecular Formula:
    5. Molecular Weight: 887.889
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874905-04-1.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: C43H53NO19(CAS DataBase Reference)
    10. NIST Chemistry Reference: C43H53NO19(874905-04-1)
    11. EPA Substance Registry System: C43H53NO19(874905-04-1)
  • 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: 874905-04-1(Hazardous Substances Data)

874905-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874905-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,9,0 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 874905-04:
(8*8)+(7*7)+(6*4)+(5*9)+(4*0)+(3*5)+(2*0)+(1*4)=201
201 % 10 = 1
So 874905-04-1 is a valid CAS Registry Number.

874905-04-1Downstream Products

874905-04-1Relevant articles and documents

Reinvestigation of the C5-acetamide sialic acid donor for α-selective sialylation: Practical procedure under microfluidic conditions

Uchinashi, Yosuke,Nagasaki, Masahiro,Zhou, Jiazhou,Tanaka, Katsunori,Fukase, Koichi

, p. 7243 - 7248 (2011)

Despite the previous literature describing the "low-to-modest" efficiency, the readily available C5-acetamide donor was reinvestigated for its use in α-sialylation under microfluidic conditions. The N-phenyltrifluoroacetimidate donor was efficiently mixed with an appropriate amount of TMSOTf to produce the α(2-6) and α(2-3)-sialylation products of galactose and glucosamine acceptors in excellent yields and with nearly perfect α-selectivity.

Efficient synthesis of the disialylated tetrasaccharide motif in N-glycans through an amide-protection strategy

Zhou, Jiazhou,Manabe, Yoshiyuki,Tanaka, Katsunori,Fukase, Koichi

, p. 1436 - 1440 (2016)

A disialylated tetrasaccharide, Neu5Ac(α2,3)Gal(β1,3)[Neu5Ac(α2,6)]GlcNAc (1), which is found at the termini of some N-glycans, has been synthesized. Compound 1 was obtained through an α-sialylation reaction between a sialic acid donor and a trisaccharide

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