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4-Cyanotetrahydropyran

4-Cyanotetrahydropyran Structure
CAS No.
1836-77-7
Chemical Name:
4-Cyanotetrahydropyran
Synonyms
CNP;mc338;mo338;Mo 338;mc1478;MC 338;Mc 1478;cnp1032;Cnp 1032;Chlonitrofen
CBNumber:
CB4308470
Molecular Formula:
C12H6Cl3NO3
Molecular Weight:
318.54
MOL File:
1836-77-7.mol
MSDS File:
SDS
Modify Date:
2023/5/4 17:34:35

4-Cyanotetrahydropyran Properties

Melting point 105-106°
Boiling point 206°C (rough estimate)
Density 1.533
refractive index 1.6200 (estimate)
storage temp. 0-6°C
color Pale yellow needles
Water Solubility 764ug/L(22 ºC)
BRN 1890443
EPA Substance Registry System Chlornitrofen (1836-77-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P501
Hazard Codes  Xi,F,N
Risk Statements  50/53
Safety Statements  60-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
HS Code  2904200090
Toxicity LC50 in carp (48 hr): >10,000 mg/l; LC50 in flea (3 hr): >40,000 mg/l (Kanazawa)

4-Cyanotetrahydropyran Chemical Properties,Uses,Production

Uses

Herbicide.

Safety Profile

Low toxicity by ingestion and skincontact. Mutation data reported. Used as an herbicide.When heated to decomposition it emits very toxic fumesof NOx and Clí.

Metabolic pathway

Degradation of chlornitrofen by microorganisms isolated from soils gives rise to the reduction of the nitro group of chlornitrofen to the amino analog, and the successive N-acetylation or N-methylation and the cleavage of the ether linkage are dominant metabolic pathways. The metabolic pathways, however, differ depending on microorganisms and the media. The replacement of the amino group by hydroxyl group, the reduction and successive formylation of p-nitrophenol, and the cleavage of the phenyl ring ultimately to produce CO2 are also observed.

4-Cyanotetrahydropyran Preparation Products And Raw materials

Raw materials

Preparation Products

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1,3,5-trichloro-2-(4-nitrophenoxy)-benzen 1,3,5-Trichloro-2-(4-nitrophenoxy)benzene 1-Nitro-4-(2,4,6-trichlorophenoxy)benzene ether,p-nitrophenyl2,4,6-trichlorophenyl Mc 1478 MC 338 mc1478 mc338 Mo 338 mo338 p-Nitrophenyl 2,4,6-trichlorophenyl ether p-nitrophenyl2,4,6-trichlorophenylether CNP CHLORNITROFEN C.N.P;2,4,6-Trichlorophenyl-4ˊ-nitrophenylether TETRAHYDRO-2H-PYRAN-4-CARBONITRILE CHLORNITROPHEN 2,4,6-trichloro-4’-nitrodiphenylether 2',4',6'-Trichloro-4-nitrobiphenyl ether 2,4,6-Trichloro-4'-nitrodiphenyl ether 2,4,6-Trichlorophenyl 4-nitrophenyl ether 2,4,6-Trichlorophenyl p-nitrophenyl ether 2,4,6-trichlorophenyl4-nitrophenylether 2’,4’,6’-trichloro-4-nitrobiphenylether Benzene, 1,3,5-trichloro-2-(4-nitrophenoxy)- Cnp 1032 cnp1032 Diphenyl ether, 2,4,6-trichloro-4'-nitro Ether, p-nitrophenyl 2,4,6-trichlorophenyl Chlonitrofen CHLORONITROFEN 4-Nitrophenyl 2,4,6-trichlorophenyl ether 2,4,6-Trichlorophenyl-4'-nitrophenyl ether@1000 μg/mL in Isooctane Chlornitrofen@100 μg/mL in Acetonitrile 4-Cyanotetrahydropyran ISO 9001:2015 REACH 1836-77-7 90-32-6