Cas 110956-96-2,2,4-Oxazolidinedione, 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-(1-methylethylidene)-

110956-96-2

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Basic information

Product Name: 2,4-Oxazolidinedione, 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-(1-methylethylidene)-
Synonyms:
CAS NO:110956-96-2
Molecular Formula: C12H9ClFNO4
Molecular Weight: 285.659
EINECS: N/A
Product Categories: N/A
Mol File: 110956-96-2.mol

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: 2,4-Oxazolidinedione, 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-(1-methylethylidene)-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-Oxazolidinedione, 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-(1-methylethylidene)-(110956-96-2)
EPA Substance Registry System: 2,4-Oxazolidinedione, 3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-(1-methylethylidene)-(110956-96-2)

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: 110956-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110956-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,5 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110956-96:
(8*1)+(7*1)+(6*0)+(5*9)+(4*5)+(3*6)+(2*9)+(1*6)=122
122 % 10 = 2
So 110956-96-2 is a valid CAS Registry Number.

110956-96-2Upstream product

110956-96-2Downstream Products

129143-39-1 3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropyl-1,3-oxazolidine-2,4-dione

110956-96-2Relevant academic research and scientific papers

Oxazolidinedione derivatives, method of producing the derivatives, and herbicides containing the derivatives

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, (2008/06/13)

Disclosed are novel oxazolidinedione derivatives expressed by the following formula: STR1 (R1, R2, R3, R4 and R5 being defined in the specification), a method of producing the derivatives and herbicides containing the derivatives as an active ingredient. These novel derivatives exhibit excellent weed-killing activity for harmful weeds and low phytotoxicity for crops.

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