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1H-INDAZOL-4-AMINE

Product Name
1H-INDAZOL-4-AMINE
CAS No.
41748-71-4
Chemical Name
1H-INDAZOL-4-AMINE
Synonyms
4-Aminoindazole;1H-INDAZOL-4-AMINE;4-AMINO (1H)INDAZOLE;1H-indazol-4-ylamine;1H-Indazol-4-amine ,97%;4-Amine-1H-Indazole, 97%;1H-Indazol-4-amine (9CI, ACI);1H-indazol-4-amine(SALTDATA: FREE)
CBNumber
CB2448361
Molecular Formula
C7H7N3
Formula Weight
133.15
MOL File
41748-71-4.mol
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1H-INDAZOL-4-AMINE Property

Melting point:
148-150°C
Boiling point:
376.6±15.0 °C(Predicted)
Density 
1.367±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
15.61±0.40(Predicted)
Appearance
Light yellow to brown Solid
InChI
InChI=1S/C7H7N3/c8-6-2-1-3-7-5(6)4-9-10-7/h1-4H,8H2,(H,9,10)
InChIKey
MDELYEBAXHZXLZ-UHFFFAOYSA-N
SMILES
N1C2=C(C(N)=CC=C2)C=N1
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Safety

Hazard Codes 
Xn
Risk Statements 
34-22-36/37/38
Safety Statements 
26-36/37/39-22
RIDADR 
3259
HazardClass 
IRRITANT
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
I509005
Product name
1H-Indazol-4-amine
Packaging
1g
Price
$75
Updated
2021/12/16
Matrix Scientific
Product number
044540
Product name
1H-Indazol-4-amine
Purity
>95%
Packaging
5g
Price
$96
Updated
2021/12/16
Matrix Scientific
Product number
044540
Product name
1H-Indazol-4-amine
Purity
>95%
Packaging
1g
Price
$27
Updated
2021/12/16
Apolloscientific
Product number
OR16942
Product name
4-Amino-1H-indazole
Packaging
1g
Price
$43
Updated
2021/12/16
SynQuest Laboratories
Product number
3H30-1-C9
Product name
4-Amino-1H-indazole
Packaging
1g
Price
$47
Updated
2021/12/16
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1H-INDAZOL-4-AMINE Chemical Properties,Usage,Production

Chemical Properties

Grey solid

Synthesis

2942-40-7

41748-71-4

The general procedure for the synthesis of 4-aminoindazole from 4-nitroindazole is as follows: 1. 2-Methyl-3-nitroaniline (2.27 g, 14.91 mmol) was dissolved in acetic acid (60 mL) and an aqueous solution of sodium nitrite (1.13 g, 1.1 eq.) was added (5 mL). After 2 hours of reaction, the dark red solution was poured into ice/water and the precipitate was collected by filtration to give 4-nitro-1H-indazole (1.98 g, 81% yield). 2. 4-Nitro-1H-indazole (760 mg, 4.68 mmol), charcoal-loaded palladium (10%, catalyst), and ethanol (30 mL) were stirred under a hydrogen balloon for 4 hours. Upon completion of the reaction, the solvent was removed in vacuum by filtration through diatomaceous earth to afford 1H-indazol-4-ylamine (631 mg, 100% yield). 3. A suspension of 1H-indazol-4-ylamine (63 mg, 4.74 mmol) in 6 M hydrochloric acid (7.2 mL) was added dropwise to an aqueous solution (2 mL) of sodium nitrite (337 mg, 4.89 mmol) at below 0 °C. After stirring for 30 min, sodium tetrafluoroborate (724 mg) was added. The reaction mixture formed a viscous solution, which was filtered and washed briefly with water to give 1H-indazole-4-diazotetrafluoroborate (218 mg, 20% yield) as a dark red solid. 4. Dry methanol (4 mL) was purged with argon for 5 min and 1H-indazole-4-diazotetrafluoroborate (218 mg, 0.94 mmol), bis(pinacolato)diboron (239 mg, 1.0 eq.), and [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) chloride (20 mg) were added. The reaction mixture was stirred for 5 hours and then filtered through diatomaceous earth. The residue was purified by fast chromatography to afford the target product 4-aminoindazole (117 mg).

References

[1] Patent: WO2006/46031, 2006, A1. Location in patent: Page/Page column 31-33
[2] Patent: WO2007/42806, 2007, A1. Location in patent: Page/Page column 32-33
[3] Patent: US2008/76768, 2008, A1. Location in patent: Page/Page column 9
[4] Patent: US2008/76758, 2008, A1. Location in patent: Page/Page column 74
[5] Patent: WO2012/82997, 2012, A1. Location in patent: Page/Page column 78

1H-INDAZOL-4-AMINE Preparation Products And Raw materials

Raw materials

Preparation Products

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1H-INDAZOL-4-AMINE Suppliers

Huzhou Huanyu Biotechnology Co. , Ltd.
Tel
18994340517
Email
709951195@qq.com
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China
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53
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58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
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China
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96815
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Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
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China
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44801
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Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
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56
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9883
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59
ZEROSCHEM.CO.,LTD.
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10-61256048 13810278579
Fax
+86 10 61256049
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sales@zeroschem.com
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China
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1370
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Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
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China
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15883
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Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
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China
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42934
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China DongFan Chemical Co.,LTD
Tel
86-0571-85151182
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86-0571-85151182
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China
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5691
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SpringPharma Tech Co.,Ltd
Tel
+86-25-68710855, +86-25-68710897
Fax
025-68710856
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sales@springpharma.net
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China
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1261
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View Lastest Price from 1H-INDAZOL-4-AMINE manufacturers

Career Henan Chemical Co
Product
1H-INDAZOL-4-AMINE 41748-71-4
Price
US $8.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10tons
Release date
2018-12-24