Cas 230313-38-9,(S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester

230313-38-9

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Basic information

Product Name: (S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester
Synonyms: (S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester
CAS NO:230313-38-9
Molecular Formula:
Molecular Weight: 372.309
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: (S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester(230313-38-9)
EPA Substance Registry System: (S)-N-phthaloyl-3-(4-fluoro-3-nitrophenyl)alanine methyl ester(230313-38-9)

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: 230313-38-9(Hazardous Substances Data)

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230313-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 230313-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,3,1 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 230313-38:
(8*2)+(7*3)+(6*0)+(5*3)+(4*1)+(3*3)+(2*3)+(1*8)=79
79 % 10 = 9
So 230313-38-9 is a valid CAS Registry Number.

230313-38-9Upstream product

230313-38-9Downstream Products

230313-39-0 (2S,3RS)-N-phthaloyl-3-bromo-3-(4-fluoro-3-nitrophenyl)alanine methyl ester

230313-38-9Relevant academic research and scientific papers

Synthesis of beta-hydroxy-beta-(fluoronitrophenyl)alanines: vital components in the assembly of biologically active cyclic peptides.

Hutton

, p. 295 - 297 (1999)

[formula: see text] Numerous biologically active cyclic peptides, such as the antibiotic vancomycin, contain amino acid residues connected through side-chain biaryl or aryl-alkyl ether linkages. Nucleophilic aromatic substitution reactions have recently b

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