Cas 1214738-01-8,(3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one

1214738-01-8

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Basic information

Product Name: (3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one
Synonyms: (3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one
CAS NO:1214738-01-8
Molecular Formula:
Molecular Weight: 503.595
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: (3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one(1214738-01-8)
EPA Substance Registry System: (3R,4aR,5R,6R,7R)-5,6-bis(benzyloxy)-7-(benzyloxy-methyl)-3-(hydroxymethyl)hexahydro-1H-pyrrolo[1,2-c][1,3]oxazin-1-one(1214738-01-8)

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: 1214738-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1214738-01-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,3 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1214738-01:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*3)+(3*8)+(2*0)+(1*1)=128
128 % 10 = 8
So 1214738-01-8 is a valid CAS Registry Number.

1214738-01-8Upstream product

1214737-97-9 (2R,3R,4R,5R)-benzyl 3,4-bis(benzyloxy)-2-(benzyloxy-methyl)-5-((R)-2,3-dihydroxypropyl)pyrrolidine-1-carboxylate

1214738-01-8Downstream Products

1214738-01-8Relevant academic research and scientific papers

Synthesis of d-arabinose-derived polyhydroxylated pyrrolidine, indolizidine and pyrrolizidine alkaloids. Total synthesis of hyacinthacine A2

Delso, Ignacio,Tejero, Tomás,Goti, Andrea,Merino, Pedro

experimental part, p. 1220 - 1227 (2010/04/02)

Several new polyhydroxylated alkaloids including pyrrolidines with a long side chain and 3-(hydroxymethyl) indolizidines were prepared from a common nitrone easily obtained from d-arabinose. In addition, a total synthesis of hyacinthacine A2 has been achieved in five steps and 67.7% overall yield starting from the same d-arabino-derived nitrone. All synthesized compounds have a common structural feature consisting of a pyrrolidine ring with d-arabino configuration.

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