Cas 714222-60-3,(+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate

714222-60-3

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Basic information

Product Name: (+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate
Synonyms: (+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate
CAS NO:714222-60-3
Molecular Formula:
Molecular Weight: 597.78
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: (+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate(714222-60-3)
EPA Substance Registry System: (+/-)-methyl N-benzoyl-α-(E)-(2'-fluoro-2'-benzenesulfonyl)vinyl-(3''-O-tert-butyldimethylsilyl)-m-tyrosinate(714222-60-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 714222-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 714222-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,4,2,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 714222-60:
(8*7)+(7*1)+(6*4)+(5*2)+(4*2)+(3*2)+(2*6)+(1*0)=123
123 % 10 = 3
So 714222-60-3 is a valid CAS Registry Number.

714222-60-3Upstream product

714222-60-3Downstream Products

714222-60-3Relevant academic research and scientific papers

Synthesis of quaternary amino acids bearing a (2′Z)-fluorovinyl α-branch: Potential PLP enzyme inactivators

Berkowitz, David B.,De La Salud-Bea, Roberto,Jahng, Wan-Jin

, p. 1821 - 1824 (2007/10/03)

Matrix presented. Protected α-formyl amino acids, themselves available from the corresponding α-vinyl amino acids, are stereoselectively transformed into the (2)-configured α-(2′-fluoro) vinyl amino acids via a three-step sequence. The route employs McCar

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