Cas 1352405-65-2,(3S,7aR)-methyl 7-((3R,4R,1Z)-5-(benzyloxy)-4-hydroxy-3-methylpent-1-enyl)-3-tert-butyl-6-methyl-5-oxo-1,3,5,7a-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylate

1352405-65-2

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Basic information

Product Name: (3S,7aR)-methyl 7-((3R,4R,1Z)-5-(benzyloxy)-4-hydroxy-3-methylpent-1-enyl)-3-tert-butyl-6-methyl-5-oxo-1,3,5,7a-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylate
Synonyms:
CAS NO:1352405-65-2
Molecular Formula:
Molecular Weight: 457.567
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,7aR)-methyl 7-((3R,4R,1Z)-5-(benzyloxy)-4-hydroxy-3-methylpent-1-enyl)-3-tert-butyl-6-methyl-5-oxo-1,3,5,7a-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,7aR)-methyl 7-((3R,4R,1Z)-5-(benzyloxy)-4-hydroxy-3-methylpent-1-enyl)-3-tert-butyl-6-methyl-5-oxo-1,3,5,7a-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylate(1352405-65-2)
EPA Substance Registry System: (3S,7aR)-methyl 7-((3R,4R,1Z)-5-(benzyloxy)-4-hydroxy-3-methylpent-1-enyl)-3-tert-butyl-6-methyl-5-oxo-1,3,5,7a-tetrahydropyrrolo[1,2-c]oxazole-7a-carboxylate(1352405-65-2)

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: 1352405-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352405-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,4,0 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1352405-65:
(9*1)+(8*3)+(7*5)+(6*2)+(5*4)+(4*0)+(3*5)+(2*6)+(1*5)=132
132 % 10 = 2
So 1352405-65-2 is a valid CAS Registry Number.

1352405-65-2Upstream product

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1352405-65-2Relevant academic research and scientific papers

Formal synthesis of (+)-neooxazolomycin via a Stille cross-coupling/ deconjugation route

Bastin, Reyhan,Dale, James W.,Edwards, Michael G.,Papillon, Julien P.N.,Webb, Michael R.,Taylor, Richard J.K.

, p. 10026 - 10044 (2012/02/13)

A formal synthesis of neooxazolomycin is described via the preparation of Kende's key intermediate in a longest linear sequence of 23 steps. This work is founded upon the union of three fragments: Moloney's lactam-derived triflate, a vinyl stannane and a

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