Cas 137910-15-7,(3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one

137910-15-7

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Basic information

Product Name: (3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one
Synonyms: (3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one
CAS NO:137910-15-7
Molecular Formula:
Molecular Weight: 421.494
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: (3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one(137910-15-7)
EPA Substance Registry System: (3S,6S)-2-((2R,5R)-2,5-Bis-methoxymethyl-pyrrolidine-1-carbonyl)-6-isopropoxy-3-phenyl-[1,2,5]oxadiazinan-4-one(137910-15-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 137910-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137910-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137910-15:
(8*1)+(7*3)+(6*7)+(5*9)+(4*1)+(3*0)+(2*1)+(1*5)=127
127 % 10 = 7
So 137910-15-7 is a valid CAS Registry Number.

137910-15-7Upstream product

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137910-15-7Relevant academic research and scientific papers

Asymmetric Amination of Carboxylic Acids via a Diels-Alder Strategy.

Gouverneur, Veronique,Ghosez, Leon

, p. 5349 - 5352 (1991)

2-Azadienes 1 which are readily prepared from acyl chlorides react with high facial selectivity with the chiral carbamoyl nitroso dienophile 2.Reduction and hydrolysis of the adducts yield enantiomerically pure amino acids.

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