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Home > Encyclopedia > 3-Methylpyridazin-6-ylhydrazine

3-Methylpyridazin-6-ylhydrazine

3-Methylpyridazin-6-ylhydrazine structure

3-Methylpyridazin-6-ylhydrazine 

structure
  • CAS No:

    38956-79-5

  • Formula:

    C5H8N4

  • Chemical Name:

    3-Methylpyridazin-6-ylhydrazine

  • Synonyms:

    3-hydrazinyl-6-methylpyridazine;3-Methylpyridazin-6-Ylhydrazine;3-Hydrazino-6-methylpyridazine;3(2H)-Pyridazinone, 6-methyl-, hydrazone;(6-METHYLPYRIDAZIN-3-YL)HYDRAZINE;KSC719Q3B;SCHEMBL3584566;(6-methylpyridazin-3-yl)diazane;6-methylpyridazine-3-ylhydrazine;CTK1B4493

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

3-Methylpyridazin-6-ylhydrazine Basic Attributes

124.15

124.07500

DTXSID30495389

2933990090

Characteristics

63.8

-0.2

Safety Information

IRRITANT

P201, P202, P264, P270, P280, P281, P301+P312, P305+P351+P338, P308+P313, P310, P330, P405, P501

H302

|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P264, P270, P280, P281, P301+P312, P305+P351+P338, P308+P313, P310, P330, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

3-Methylpyridazin-6-ylhydrazine Use and Manufacturing

3-Hydrazino-6-methylpyridazine Hydrazine monohydrate (45 mL) was added to a suspension of 3-chloro-6-methylpyridazine (3.00 g) in ethanol (45 mL), and the resultant mixture was heated to reflux for 2.5 hours. After air cooling, a residue obtained by evaporating the solvent of the reaction solution under reduced pressure was purified by silica gel chromatography (chloroform-methanol-water (a lower layer solvent of 7: 3: 1 (v/v)), to obtain the title compound (2.35 g, 81percent) as a solid. 6-Methyl-[l, 2, 4]triazolo[4, 3-b]pyridazine-3-thioI; Step 1: (6-Methyl-pyridazin-3-yl)-hydrazine; [0372J To a suspension of 3-chloro-6-methyl-pyridazine (3 g, 23.3 mmol) in ethanol (45 mL) was added hydrazine hydrate (45 mL) and the resultant mixture was heated to reflux for 3 hrs. Most of the solvent was removed under reduced pressure and the white solid was collected by filtration and washed with ethanol. Upon drying 2.3 g of (6-methyl-pyridazin- 3 -yl) -hydrazine was obtained as a white crystalline solid (80percent yield).1) 3-Hydrazino-6-methylpyridazine Hydrazine monohydrate (45 mL) was added to a suspension of 3-chloro-6-methylpyridine (3.00 g) in ethanol (45 mL), and the resultant mixture was heated to reflux for 2.5 hours. After air cooling, a residue obtained by evaporating the reaction solvent was purified by silica gel chromatography (a lower layer mixed solvent of chloroform-methanol-water (7:3:1)), to obtain 3-hydrazino-6-methylpyridazine (2.35 g, 81percent) as a solid.

Computed Properties

Molecular Weight:124.14
XLogP3:-0.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:124.074896272
Monoisotopic Mass:124.074896272
Topological Polar Surface Area:63.8
Heavy Atom Count:9
Complexity:85
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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