Cas 500757-03-9,N-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide

500757-03-9

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Basic information

Product Name: N-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide
Synonyms: N-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide
CAS NO:500757-03-9
Molecular Formula:
Molecular Weight: 487.291
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-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide(500757-03-9)
EPA Substance Registry System: N-((4aR,5aR,6S,8aS,9S,9aR)-9-Iodo-2,2,6-trimethyl-7-oxo-octahydro-furo[2',3':5,6]pyrano[3,2-d][1,3]dioxin-6-yl)-benzamide(500757-03-9)

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: 500757-03-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 500757-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 500757-03:
(8*5)+(7*0)+(6*0)+(5*7)+(4*5)+(3*7)+(2*0)+(1*3)=119
119 % 10 = 9
So 500757-03-9 is a valid CAS Registry Number.

500757-03-9Upstream product

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500757-03-9Relevant academic research and scientific papers

Practical stereoselective synthesis of α-D-C-mannosyl-(R)-alanine

Colombo, Lino,Di Giacomo, Marcello,Ciceri, Paola

, p. 9381 - 9386 (2007/10/03)

α-D-C-Mannosyl-(R)-alanine 2 was synthesized in only four steps starting from the known acetonide protected D-ribo-hex-1-enitol 4 and N-benzoylalanine. The key C-C bond formation between the sugar and the amino acid moieties was effected through a Claisen rearrangement of the intermediate oxazole 7, derived from the ester 6.

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