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3-[4-(Trifluoromethoxy)phenyl]-1H-pyrazole 97% is a chemical compound with the molecular formula C10H7F3N2O. It is a derivative of 1H-pyrazole, featuring a trifluoromethoxy group attached to a phenyl ring, which is in turn connected to the pyrazole nucleus. 3-[4-(Trifluoromethoxy)phenyl]-1H-pyrazole 97% is typically used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, due to its unique structure and reactivity. The 97% purity indicates that the product contains a high percentage of the desired compound, with only a small amount of impurities.

474707-71-6

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474707-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 474707-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,7,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 474707-71:
(8*4)+(7*7)+(6*4)+(5*7)+(4*0)+(3*7)+(2*7)+(1*1)=176
176 % 10 = 6
So 474707-71-6 is a valid CAS Registry Number.

474707-71-6Downstream Products

474707-71-6Relevant academic research and scientific papers

3-aryl azabicyclo derivative as well as preparation and application thereof in nematode killing

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Paragraph 0160-0161, (2021/08/06)

The invention relates to preparation of a 3-aryl azabicyclo derivative and application of the derivative in nematode killing. Specifically, the invention discloses application of a compound with a structure as shown in a formula (I) or a composition, an optical isomer, a cis-trans-isomer and an agricultural pharmacologically acceptable salt of the compound in the field of nematode killing.

NITROGENOUS FUSED?RING COMPOUND HAVING PYRAZOLYL GROUP AS SUBSTITUENT AND MEDICINAL COMPOSITION THEREOF

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Page 87, (2008/06/13)

The present invention provides a compound having an excellent inhibitory action on activation of STAT6 and a pharmaceutical composition thereof. Inparticular, it provides a compound represented by the following formula (I), a salt thereof or a hydrate of them. In the formula, X represents a nitrogen-containing condensed aromatic heterocyclic group such as imidazo[1,2-a]pyridine, benzimidazole, quinazoline, quinoline, or 2,1-benzisoxazole and has (R4)n as substituent groups; Y represents a C3-8 cycloalkyl group, C4-8 cycloalkenyl group, 5- to 14-membered non-aromatic heterocyclic group, C6-14 aromatic hydrocarbon cyclic group or 5- to 14-membered aromatic heterocyclic group; n in (R4)n is 0, 1, 2 or 3, and Z groups independently represent (1) hydrogen atom, (2) amino group, (3) halogen atom, (4) hydroxyl group, (5) nitro group, (6) cyano group, (7) azido group, (8) formyl group, (9) hydroxyamino group, (10) sulfamoyl group, (11) guanodino group, (12) oxo group, (13) C2-6 alkenyl group, (14) C1-6 alkoxy group, (15) C1-6 alkylhydroxyamino group, (16) halogenated C1-6 alkyl group, (17) halogenated C2-6 alkenyl group, (18) (i) C3-7cycloalkyl group, (ii) C3-7cycloalkenyl group, (iii) 5- to 14-membered non-aromatic heterocyclic group, each of which may have one or more substituent groups Q, or (19) formula -M1-M2-M3, R1 represents (1) hydrogen atom, (2) halogen atom, (3) hydroxyl group, (4) nitro group, (5) cyano group, (6) halogenated C1-6 alkyl group, (7) C2-6 alkyl group substituted with a hydroxyl or cyano group, (8) C2-6 alkenyl group, or (9) formula -L1-L2-L3, and R2 represents a hydrogen atom or a protecting group; and R3 represents a hydrogen atom, halogen atom, cyano group, amino group, C1-4 alkyl group or halogenated C1-4 alkyl group.

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