Cas 1125812-35-2,1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one

1125812-35-2

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Basic information

Product Name: 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one
Synonyms: 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one
CAS NO:1125812-35-2
Molecular Formula:
Molecular Weight: 474.104
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: 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one(1125812-35-2)
EPA Substance Registry System: 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-2-buten-1-one(1125812-35-2)

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: 1125812-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1125812-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,5,8,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1125812-35:
(9*1)+(8*1)+(7*2)+(6*5)+(5*8)+(4*1)+(3*2)+(2*3)+(1*5)=122
122 % 10 = 2
So 1125812-35-2 is a valid CAS Registry Number.

1125812-35-2Upstream product

1125724-14-2 1-(4-bromo-1-naphthalenyl)-3-(3,5-dichlorophenyl)-4,4,4-trifluoro-3-hydroxy-1-butanone

1125812-35-2Downstream Products

943847-23-2 3-(4-bromo-1-naphthalenyl)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)isoxazole

1125812-35-2Relevant academic research and scientific papers

METHOD FOR PREPARING 5-HALOALKYL-4,5-DIHYDROISOXAZOLE DERIVATIVES

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Page/Page column 38, (2009/04/25)

Disclosed is a method for preparing a compound of Formula: (1); wherein R1 is CHX2, CX3, CX2CHX2 or CX2CX3; each X is independently Cl or F; Z is optionally substituted phenyl; and Q is phenyl or 1-naphthalenyl, each optionally substituted as defined in the disclosure; comprising contacting a compound of Formula: (2).

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