Cas 147749-05-1,methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate

147749-05-1

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Basic information

Product Name: methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate
Synonyms: methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate
CAS NO:147749-05-1
Molecular Formula: C12H10F3NO4
Molecular Weight: 289.2073096
EINECS: N/A
Product Categories: N/A
Mol File: 147749-05-1.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate(CAS DataBase Reference)
NIST Chemistry Reference: methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate(147749-05-1)
EPA Substance Registry System: methyl [3-hydroxy-2-oxo-3-(trifluoromethyl)-2,3-dihydro-1H-indol-1-yl]acetate(147749-05-1)

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: 147749-05-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147749-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,7,4 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147749-05:
(8*1)+(7*4)+(6*7)+(5*7)+(4*4)+(3*9)+(2*0)+(1*5)=161
161 % 10 = 1
So 147749-05-1 is a valid CAS Registry Number.

147749-05-1Upstream product

147749-05-1Downstream Products

147749-05-1Relevant articles and documents

HEXAFLUOROACETONE AND METHYL TRIFLUOROPYRUVATE AS PRECURSORS OF MODIEFIED ESTERS OF N-ACYL-N-PHENYL-α-AMINO ACIDS

Chkanikov, N. D.,Sviridov, V. D.,Zelenin, A. E.,Tyutin, V. Yu.,Kolomiets, A. F.,Fokin, A. V.

, p. 1415 - 1424 (2007/10/02)

The C-oxyalkylation of N-aryl-α-amino acids by hexafluoroacetone (1) and methyl trifluoropyruvate (2), followed by acylation of the products 3-13, 15, and 17 formed, was carried out.The activity of the synthesized anilides against pathogens of plant fungu

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