3-Chloro-6-hydrazinopyridazine

Modify Date: 2025-08-27 17:58:05

3-Chloro-6-hydrazinopyridazine structure	Common Name	3-Chloro-6-hydrazinopyridazine
	CAS Number	17284-97-8	Molecular Weight	144.56200
	Density	1.53 g/cm3	Boiling Point	402.2ºC at 760 mmHg
	Molecular Formula	C₄H₅ClN₄	Melting Point	137-141 °C(lit.)
	MSDS	Chinese USA	Flash Point	197ºC
	Symbol	GHS05, GHS07	Signal Word	Danger

Name	3-Chloro-6-hydrazinopyridazine
Synonym	More Synonyms

Density	1.53 g/cm3
Boiling Point	402.2ºC at 760 mmHg
Melting Point	137-141 °C(lit.)
Molecular Formula	C₄H₅ClN₄
Molecular Weight	144.56200
Flash Point	197ºC
Exact Mass	144.02000
PSA	63.83000
LogP	1.18890
Vapour Pressure	0mmHg at 25°C
Index of Refraction	1.684
InChIKey	FXYQRYGWWZKUFV-UHFFFAOYSA-N
SMILES	NNc1ccc(Cl)nn1

3-Chloro-6-hydrazinopyridazine MSDS(Chinese)

Symbol	GHS05, GHS07
Signal Word	Danger
Hazard Statements	H302-H317-H318
Precautionary Statements	P280-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes	Xn:Harmful;
Risk Phrases	R22;R41;R43
Safety Phrases	S37/39
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2942000000

3,6-Dichloropyr...

CAS#:141-30-0

~99%

3-Chloro-6-hydr...

CAS#:17284-97-8

Literature: Guetzoyan, Lucie; Ingham, Richard J.; Nikbin, Nikzad; Rossignol, Julien; Wolling, Michael; Baumert, Mark; Burgess-Brown, Nicola A.; Strain-Damerell, Claire M.; Shrestha, Leela; Brennan, Paul E.; Fedorov, Oleg; Knapp, Stefan; Ley, Steven V. MedChemComm, 2014 , vol. 5, # 4 p. 540 - 546

6-chloropyridaz...

CAS#:3916-78-7

3-Chloro-6-hydr...

CAS#:17284-97-8

Literature: Yakugaku Zasshi, , vol. 76, p. 1293,1295 Chem.Abstr., , p. 6645

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

(Z)-3-(4-bromophenyl)-3-(3-pyridyl)allylamine as substrate for studies of myeloperoxidase activity.

Chem. Biol. Interact. 94(2) , 83-99, (1995)

(Z)-3-(4-Bromophenyl)-3-(3-pyridyl)allylamine (CPP 200) is transformed to the corresponding chloroimine by hypochlorite ion (ClO-) formed in the presence of myeloperoxidase. A scheme for this transfor...

Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS

Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN

Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN

Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN

Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay

Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.

Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity

Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity

Name: Fluorescence-based cell-based primary high throughput screening assay to identify pos...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_PAM_FLUO8_1536_1X%ACT PRUN

Name: Fluorescence polarization-based biochemical high throughput primary assay to identify...
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id: SIAE_INH_FP_1536_1X%INH PRUN

Total 116, Current Page 1 of 12