(2,4-Dimethylphenyl)hydrazine hydrochloride (1:1)

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Names

[ Name ]:
(2,4-Dimethylphenyl)hydrazine hydrochloride (1:1)

[Synonym ]:
ZMR B1 D1 &&HCl
MFCD00013381
2,4-Dimethylphenylhydrazine HCI
(2,4-dimethylphenyl)hydrazine hydrochloride
2,4-DIMETHYLPHENYLHYDRAZINE HCL
(2,4-Dimethylphenyl)hydrazine hydrochloride (1:1)
2,4-Dimethylphenylhydrazinehydrochloride
Hydrazine, (2,4-dimethylphenyl)-, hydrochloride (1:1)
4-Hydrazino-m-xylene hydrochloride

Chemical & Physical Properties

[ Melting Point ]:
180 °C

[ Molecular Formula ]:
C₈H₁₃ClN₂

[ Molecular Weight ]:
172.655

[ Exact Mass ]:
172.076721

[ PSA ]:
38.05000

[ LogP ]:
3.16430

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2928000090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2928000090

[ 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%

Articles

Synthesis and structure-activity relationships (SARs) of 1,5-diarylpyrazole cannabinoid type-1 (CB(1)) receptor ligands for potential use in molecular imaging.

Bioorg. Med. Chem. 14(11) , 3712-20, (2006)

Cannabinoid type-1 (CB(1)) receptor ligands, derived from the 1,5-diarylpyrazole core template of rimonabant (Acomplia), have been the focus of several studies aimed at examining structure-activity re...

The first synthesis of [11C]J147, a new potential PET agent for imaging of Alzheimer's disease.

Bioorg. Med. Chem. Lett. 23(2) , 524-7, (2013)

J147 was synthesized from 2,4-dimethylphenylhydrazine hydrochloride and 3-methoxybenzaldehyde in 2 steps with 71% overall yield. The precursor desmethyl-J147 was synthesized from 3-hydroxybenzaldehyde...

(3,4-Dimethylphenyl)hydrazine hydrochloride (1:1)
4-Morpholinepropanol, a-(2,4-dimethylphenyl)-,hydrochloride (1:1)
1-Propanone,3-(3-azabicyclo[3.2.2]non-3-yl)-1-(2,4-dimethylphenyl)-, hydrochloride (1:1)
(2,4-Difluorophenyl)hydrazine hydrochloride (1:1)
(2,4-Dimethylphenyl)hydrazine
(2,4-Difluorophenyl)hydrazinium chloride
3-[3-(benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-3-cyclobutylpropanoic acid
3-cyclobutyl-3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]propanoic acid
3-cyclobutyl-3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]propanoic acid
4-(1H-pyrazol-1-yl)-6-(4-{[5-(trifluoromethyl)-1,3,4-oxadiazol-2-yl]methyl}piperazin-1-yl)pyrimidine
(2S)-2-[(2S)-3-(dimethylamino)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]-4-(methylsulfanyl)butanoic acid
(2S)-3-(dimethylamino)-2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]propanoic acid
3-[N-ethyl-4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methoxybutanamido]propanoic acid
2-[(2R)-1-{1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclopropanecarbonyl}piperidin-2-yl]acetic acid
2-[(2S)-1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylbutanoyl]piperidin-2-yl]acetic acid
3-({5-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]oxolan-3-yl}formamido)-2,2-dimethylpropanoic acid

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