4-Chlorophenylhydrazine hydrochloride structure
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Common Name | 4-Chlorophenylhydrazine hydrochloride | ||
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CAS Number | 1073-70-7 | Molecular Weight | 179.047 | |
Density | 1.32g/cm3 | Boiling Point | 265.3ºC at 760mmHg | |
Molecular Formula | C6H8Cl2N2 | Melting Point | 216 °C (dec.)(lit.) | |
MSDS | Chinese USA | Flash Point | 114.2ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | 4-Chlorophenylhydrazine hydrochloride |
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Synonym | More Synonyms |
Density | 1.32g/cm3 |
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Boiling Point | 265.3ºC at 760mmHg |
Melting Point | 216 °C (dec.)(lit.) |
Molecular Formula | C6H8Cl2N2 |
Molecular Weight | 179.047 |
Flash Point | 114.2ºC |
Exact Mass | 178.006454 |
PSA | 38.05000 |
LogP | 3.20090 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H312-H332 |
Precautionary Statements | P280 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn:Harmful |
Risk Phrases | R20/21/22 |
Safety Phrases | S36/37 |
RIDADR | 2811 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 29280090 |
~63% 4-Chlorophenylh... CAS#:1073-70-7 |
Literature: Chinese Journal of Chemistry, , vol. 30, # 4 p. 919 - 923 |
~% 4-Chlorophenylh... CAS#:1073-70-7 |
Literature: Tetrahedron, , vol. 67, # 52 p. 10296 - 10303 |
~88% 4-Chlorophenylh... CAS#:1073-70-7 |
Literature: Journal of the Chinese Chemical Society, , vol. 47, # 1 p. 227 - 240 |
Precursor 2 | |
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DownStream 9 | |
HS Code | 2928000090 |
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Summary | 2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0% |
Reaction of 3-acetonyl-5-cyano-1,2,4-thiadiazole with phenylhydrazine hydrochlorides: indolization and phenylpyrazolation.
Chem. Pharm. Bull. 48(1) , 160-2, (2000) Treatment of 3-acetonyl-5-cyano-1,2,4-thiadiazole (1) with 4-methyl or 4-methoxyphenylhydrazine hydrochloride provided 5-cyano-3-(2,5-dimethylindol-3-yl)-1,2,4-thiadiazole (2) or 5-cyano-3-(5-methoxy-... |
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Reactions of prostaglandin H synthase with monosubstituted hydrazines and diazenes. Formation of iron(II)-diazene and iron(III)-sigma-alkyl or iron(III)-sigma-aryl complexes.
Eur. J. Biochem. 226(2) , 445-57, (1994) The reaction of p-chlorophenylhydrazine with prostaglandin H synthase (PGHS) Fe(III) under aerobic conditions leads to a partial destruction of the heme and to a new complex absorbing at 436 nm. This ... |
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Design, synthesis and biological evaluation of indane-2-arylhydrazinylmethylene-1,3-diones and indol-2-aryldiazenylmethylene-3-ones as beta-amyloid aggregation inhibitors.
Eur. J. Med. Chem. 45(4) , 1359-66, (2010) Biological screening of (hetero)aromatic compounds allowed the identification of some novel inhibitors of Abeta(1-40) aggregation, bearing indane and indole rings as common scaffolds. Molecular decora... |
Hydrazine, (4-chlorophenyl)-, monohydrochloride |
p-Chlorophenylhydrazine monohydrochloride |
4-CHLORO PHENYL HYDRAZXINE HYDROCHLORIDE |
(4-Chlorophenyl)hydrazine hydrochloride (1:1) |
4-Chlorophenylhydrazine hydrochloride |
1-(4-chlorophenyl)hydrazine hydrochloride |
Hydrazine, (p-chlorophenyl)-, monohydrochloride |
(4-chlorophenyl)hydrazine hydrochloride |
4-CHLOROPHENYLHYDRAZINE HCL |
MFCD00012943 |
EINECS 214-030-9 |
4-Chlorophenylhydrazine monohydrochloride |
4-Cl-phenylhydrazine hydrochloride |
P-CHLOROPHENYLHYDRAZINE HCL |
Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1) |
P-Chlorophenyluhydrazinehydrochloride |