Cas 773155-83-2,N-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide

773155-83-2

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Basic information

Product Name: N-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide
Synonyms: N-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide
CAS NO:773155-83-2
Molecular Formula:
Molecular Weight: 578.747
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-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide(773155-83-2)
EPA Substance Registry System: N-[1-benzyl-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-butyl]-N-(4-benzyl-2-oxo-oxazolidin-3-yl)-2,2,2-trifluoro-acetamide(773155-83-2)

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: 773155-83-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 773155-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,1,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773155-83:
(8*7)+(7*7)+(6*3)+(5*1)+(4*5)+(3*5)+(2*8)+(1*3)=182
182 % 10 = 2
So 773155-83-2 is a valid CAS Registry Number.

773155-83-2Upstream product

773155-83-2Downstream Products

773155-79-6 N-((1R,3S)-1-Benzyl-4-hydroxy-3-methyl-butyl)-2,2,2-trifluoro-acetamide

773155-83-2Relevant academic research and scientific papers

Stereoselective Mn-mediated coupling of functionalized iodides and hydrazones: A synthetic entry to the tubulysin γ-amino acids

Friestad, Gregory K.,Marie, Jean-Charles,Deveau, Amy M.

, p. 3249 - 3252 (2007/10/03)

(Chemical Equation Presented) Synthesis of γ-amino acids, important building blocks in bioorganic and natural product chemistry, is accomplished using a stereoselective carbon-carbon bond construction of the chiral amine. Alkyl iodides and chiral hydrazon

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