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61747-76-0

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61747-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61747-76-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61747-76:
(7*6)+(6*1)+(5*7)+(4*4)+(3*7)+(2*7)+(1*6)=140
140 % 10 = 0
So 61747-76-0 is a valid CAS Registry Number.

61747-76-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-N-phenyl-1H-pyrazole-4-carboxamide

1.2 Other means of identification

Product number -
Other names 3,5-dimethyl-4-phenylaminocarbonyl-1H-pyrazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61747-76-0 SDS

61747-76-0Downstream Products

61747-76-0Relevant articles and documents

Straightforward transformation of isoxazoles into pyrazoles: renewed and improved

Sviridov, Sergey I.,Vasil'ev, Andrei A.,Shorshnev, Sergey V.

, p. 12195 - 12201 (2008/02/11)

Isoxazoles bearing alkyl or carbamoyl groups were transformed into the corresponding pyrazoles in high yields by the treatment with hydrazine in methanol in the presence of a hydrogenation catalyst, e.g., Raney nickel, at ambient temperature. For the synthesis of N-substituted pyrazoles, hydrogenolysis of isoxazole followed by the treatment with substituted hydrazine was required. 3(5)-Aryl- or acylamido-substituted isoxazoles are less suitable for such transformations.

Compounds and compositions

-

, (2008/06/13)

Fungicidal compositions comprising as an active ingredient a compound of the general formula I STR1 wherein either R1 or R2 is the group STR2 in which X is an oxygen atom or a sulphur atom and R5 is straight chain alkyl group of 1 to 8 carbon atoms, branched chain alkyl group of 1 to 8 carbon atoms, cyclic alkyl group of 3 to 8 carbon atoms, alkenyl group, alkynyl group, hydroxyalkyl group phenyl group or a mono-, di- or tri- substituted phenyl group with substituents, which may be the same or different, chosen from the group consisting hydrogen alkyl, alkenyl, alkynyl, hydroxyalkyl, alkoxy, phenyl, halogen, trifluoromethyl, thiocyanate, nitro, cyano, amino, carboxy, alkoxycarbonyl, carbamoyl, N-alkylcarbamoyl and N,N-dialkylcarbamoyl; when R1 is the group STR3 then R3 is hydrogen, alkyl, alkenyl alkynyl, hydroxyalkyl, phenyl, CH2 CF3 or the group --CH2 COOR6 wherein R6 is alkyl, phenyl or substituted phenyl, and R2 and R4, which may be the same or different, are hydrogen, alkyl, alkenyl, alkynyl, hydroxalkyl, alkoxy, phenyl, halogen, trifluoromethyl, thiocyanate, nitro, cyano, amino, carboxy, alkoxycarbonyl, carbamoyl, N,alkylcarbamoyl, N,N-dialkylcarbamoyl, hydroxy or mercapto provided that R2 and R4 are not both hydrogen, hydroxy or mercapto; when R2 is the group STR4 then R3 is hydrogen, alkyl, alkenyl, alkynyl, hydroxyalkyl, phenyl or substituted phenyl, and R1 and R4, which may be the same or different, are hydrogen, alkyl, alkenyl, hydroxyalkyl, alkoxy, phenyl, substituted phenyl, halogen, trifluoromethyl, thiocyanate, nitro, cyano, amino, carboxy, alkoxycarbonyl, carbamoyl, N-alkylcarbamoyl, N,N-dialkylcarbamoyl, hydroxy or mercapto, provided that R1 and R3 are not both hydrogen and provided that R1 and R4 are not both hydroxy or mercapto; and an inert carrier material therefor.

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