Cas 756834-77-2,tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate

756834-77-2

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Basic information

Product Name: tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate
Synonyms: tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate
CAS NO:756834-77-2
Molecular Formula:
Molecular Weight: 255.357
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: tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate(756834-77-2)
EPA Substance Registry System: tert-butyl (5R)-5-[(1R)-1-methylprop-2-en-1-yl]-2,2-dimethyloxazolidine-3-carboxylate(756834-77-2)

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: 756834-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 756834-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,8,3 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 756834-77:
(8*7)+(7*5)+(6*6)+(5*8)+(4*3)+(3*4)+(2*7)+(1*7)=212
212 % 10 = 2
So 756834-77-2 is a valid CAS Registry Number.

756834-77-2Upstream product

31954-27-5 N-(tert-butoxycarbonyl)glycine methyl ester

756834-77-2Downstream Products

115566-02-4 bistramide A

756834-77-2Relevant academic research and scientific papers

Total synthesis of pseudotrienic acid B: A bioactive metabolite from Pseudomonas sp. MF 381-IODS

Amans, Dominique,Bellosta, Veronique,Cossy, Janine

, p. 5870 - 5874 (2006)

(Chemical Equation Presented) Acid advancement: An efficient and highly convergent stereoselective synthesis of pseudotrienic acid B (see structure) has been achieved. Synthetic highlights include a crotyltitanation reaction to control the stereogenic centers at C11 and C20, a cross-metathesis reaction to synthesize the triene moiety, and a Stille cross-coupling reaction to complete the assembly of the carbon framework of the natural product.

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