Cas 125541-58-4,2-Difluoromethyl-4-isobutyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid 3-methyl ester

125541-58-4

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Basic information

Product Name: 2-Difluoromethyl-4-isobutyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid 3-methyl ester
Synonyms:
CAS NO:125541-58-4
Molecular Formula:
Molecular Weight: 355.261
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-Difluoromethyl-4-isobutyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid 3-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Difluoromethyl-4-isobutyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid 3-methyl ester(125541-58-4)
EPA Substance Registry System: 2-Difluoromethyl-4-isobutyl-6-trifluoromethyl-pyridine-3,5-dicarboxylic acid 3-methyl ester(125541-58-4)

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: 125541-58-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125541-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,4 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125541-58:
(8*1)+(7*2)+(6*5)+(5*5)+(4*4)+(3*1)+(2*5)+(1*8)=114
114 % 10 = 4
So 125541-58-4 is a valid CAS Registry Number.

125541-58-4Upstream product

97898-70-9 4-Isobutyl-2,6-bis-trifluoromethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid dimethyl ester

125541-58-4Downstream Products

125541-58-4Relevant academic research and scientific papers

A Novel Dehydrofluorination of 2-(Trifluoromethyl)dihydro-3,5-pyridinedicarboxylates to 2-(Difluoromethyl)-3,5-pyridinedicarboxylates

Lee, Len F.,Stikes, Gina L.,Molyneaux, John M.,Sing, Y. Larry,Chupp, John P.,Woodard, Scott S.

, p. 2872 - 2877 (2007/10/02)

A series of 2-(trifluoromethyl)-1,4- and -3,4-dihydro-3,5-pyridinedicarboxylates 5a-y and 6a-y undergo an unprecedented dehydrofluorination upon treatment with 1,8-diazabicycloundec-7-ene (DBU), trialkylamines, or 2,6-lutidine to give the correspon

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