Cas 146668-91-9,N-((2R,4aR,6R,7S,8R,8aS)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylmethyl)-acetamide

146668-91-9

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Basic information

Product Name: N-((2R,4aR,6R,7S,8R,8aS)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylmethyl)-acetamide
Synonyms:
CAS NO:146668-91-9
Molecular Formula:
Molecular Weight: 427.497
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: N-((2R,4aR,6R,7S,8R,8aS)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylmethyl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2R,4aR,6R,7S,8R,8aS)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylmethyl)-acetamide(146668-91-9)
EPA Substance Registry System: N-((2R,4aR,6R,7S,8R,8aS)-8-Benzyloxy-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylmethyl)-acetamide(146668-91-9)

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: 146668-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146668-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,6,6 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146668-91:
(8*1)+(7*4)+(6*6)+(5*6)+(4*6)+(3*8)+(2*9)+(1*1)=169
169 % 10 = 9
So 146668-91-9 is a valid CAS Registry Number.

146668-91-9Upstream product

146668-91-9Downstream Products

146668-91-9Relevant academic research and scientific papers

Synthesis of the C-5 homologue of N-acetylneuraminic acid by enzymatic chain elongation of 2-C-acetamidomethyl-2-deoxy-D-mannose

Koppert, Klaus,Brossmer, Reinhard

, p. 8031 - 8034 (2007/10/02)

Condensation of hexopyranosid-2-ulose 1 with nitromethane afforded after acetylation 2. Treatment with borohydride yielded stereoselectively 4. Reduction, acetylation, deblocking, and acid hydrolysis gave then C-2 branched N-acetylmannosamine 7 that was e

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