Cas 444993-34-4,(R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

444993-34-4

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Basic information

Product Name: (R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
Synonyms: (R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
CAS NO:444993-34-4
Molecular Formula:
Molecular Weight: 367.445
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: (R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester(444993-34-4)
EPA Substance Registry System: (R)-4-[(E)-2-(4-Methoxy-phenyl)-vinyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester(444993-34-4)

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: 444993-34-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 444993-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,9,9 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 444993-34:
(8*4)+(7*4)+(6*4)+(5*9)+(4*9)+(3*3)+(2*3)+(1*4)=184
184 % 10 = 4
So 444993-34-4 is a valid CAS Registry Number.

444993-34-4Upstream product

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444993-34-4Relevant academic research and scientific papers

Heck reactions of amino acid building blocks: Application to the synthesis of pyrrololine analogues

Collier, Philip N.,Patel, Ian,Taylor, Richard J.K.

, p. 3401 - 3405 (2002)

Heck reactions of unsaturated amino acid building blocks are described which allow access to homo- and bis-homophenylalanine derivatives and to γ,δ-unsaturated amino acids. Preliminary synthetic studies utilising this chemistry for the preparation of pyrr

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