Cas 134297-33-9,2-<2-(4-Methylphenyl)-4-trifluoromethylthiazol-5-ylimino>-3,3,3-trifluoropropionsaeure methylester

134297-33-9

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Basic information

Product Name: 2-<2-(4-Methylphenyl)-4-trifluoromethylthiazol-5-ylimino>-3,3,3-trifluoropropionsaeure methylester
Synonyms:
CAS NO:134297-33-9
Molecular Formula:
Molecular Weight: 396.313
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-(4-Methylphenyl)-4-trifluoromethylthiazol-5-ylimino>-3,3,3-trifluoropropionsaeure methylester(CAS DataBase Reference)
NIST Chemistry Reference: 2-<2-(4-Methylphenyl)-4-trifluoromethylthiazol-5-ylimino>-3,3,3-trifluoropropionsaeure methylester(134297-33-9)
EPA Substance Registry System: 2-<2-(4-Methylphenyl)-4-trifluoromethylthiazol-5-ylimino>-3,3,3-trifluoropropionsaeure methylester(134297-33-9)

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: 134297-33-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134297-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,9 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134297-33:
(8*1)+(7*3)+(6*4)+(5*2)+(4*9)+(3*7)+(2*3)+(1*3)=129
129 % 10 = 9
So 134297-33-9 is a valid CAS Registry Number.

134297-33-9Upstream product

134297-33-9Downstream Products

134297-34-0 N-<2-(4-Methylphenyl)-4-trifluoromethylthiazol-5-yl>-3,3,3-trifluoroalaninmethylester

134297-33-9Relevant academic research and scientific papers

New Synthetic Pathways to 3,3,3-Trifluoroalanine, 2-Deutero-3,3,3-trifluoroalanine and their Derivatives

Burger, Klaus,Hoess, Eva,Gaa, Karl,Sewald, Norbert,Schierlinger, Christian

, p. 361 - 384 (2007/10/02)

New synthetic pathways to 3,3,3-trifluoroalanine, 2-deutero-3,3,3-trifluoroalanine, their esters, amides, and thioamides are described, starting from hexafluoroacetone, and trifluoropyruvates, respectively.

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