Cas 147720-69-2,2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

147720-69-2

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Basic information

Product Name: 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside
Synonyms:
CAS NO:147720-69-2
Molecular Formula:
Molecular Weight: 870.158
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside(147720-69-2)
EPA Substance Registry System: 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside(147720-69-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 147720-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147720-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,2 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147720-69:
(8*1)+(7*4)+(6*7)+(5*7)+(4*2)+(3*0)+(2*6)+(1*9)=142
142 % 10 = 2
So 147720-69-2 is a valid CAS Registry Number.

147720-69-2Upstream product

147720-69-2Downstream Products

147720-69-2Relevant academic research and scientific papers

Zinc triflate-promoted glycosidation: Synthesis of lipid A disaccharide intermediates

Nakayama,Higashi,Soga,Uoto,Kusama

, p. 2909 - 2912 (1992)

Zinc triflate was found to be superior to the heavy metal salts as a promoter in the Koenigs-Knorr type glycosidation reaction in the synthesis of lipid A disaccharide intermediates. It readily promoted the reaction of a complex glycosyl bromide with a re

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