Cas 195719-55-2,[(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester

195719-55-2

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Basic information

Product Name: [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester
Synonyms: [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester
CAS NO:195719-55-2
Molecular Formula:
Molecular Weight: 339.434
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: [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester(195719-55-2)
EPA Substance Registry System: [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid benzyl ester(195719-55-2)

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: 195719-55-2(Hazardous Substances Data)

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195719-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195719-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,7,1 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 195719-55:
(8*1)+(7*9)+(6*5)+(5*7)+(4*1)+(3*9)+(2*5)+(1*5)=182
182 % 10 = 2
So 195719-55-2 is a valid CAS Registry Number.

195719-55-2Upstream product

195719-55-2Downstream Products

195719-43-8 [(2,2-Dimethyl-propionyl)-methyl-amino]-phenyl-acetic acid

195719-55-2Relevant academic research and scientific papers

Autoxidation of intermediary mesoionic 1,3-oxazolium-5-olates generated from cyclic N-acyl α-amino acids

Kawase, Masami

, p. 1248 - 1253 (1997)

Mesoionic 1,3-oxazolium-5-olates (munchnones) react fairly rapidly with oxygen to give the autoxidation products when the C-4 substituent is aromatic. The autoxidation occurred in the munchnones generated from N-acyl tetrahydroisoquinoline-1-carboxylic ac

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