4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Base Information

Chemical Name:4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide
CAS No.:90434-92-7
Molecular Formula:C8H12 N4 O
Molecular Weight:180.209
Hs Code.:2933990090
European Community (EC) Number:696-190-3
DSSTox Substance ID:DTXSID60366972
Wikidata:Q82152498
Mol file:90434-92-7.mol

Synonyms:4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide;90434-92-7;Cambridge id 5316741;Oprea1_142073;Oprea1_844267;SCHEMBL22518533;DTXSID60366972;HMS1580G12;BBL003670;MFCD00611197;STK978822;AKOS000276471;EG-0025;SB86557;CS-0220989;FT-0683495;EN300-08081;SR-01000439001;SR-01000439001-1;Z56782953

Suppliers and Price of 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide
100mg
$ 90.00

TRC
4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide
50mg
$ 45.00

Matrix Scientific
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide
500mg
$ 315.00

Crysdot
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide 97%
5g
$ 790.00

Chemenu
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide 97%
5g
$ 746.00

Apolloscientific
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide
1g
$ 247.00

Apolloscientific
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide
500mg
$ 183.00

Apolloscientific
4,5,6,7-Tetrahydro-1H-indazole-3-carbohydrazide
5g
$ 609.00

American Custom Chemicals Corporation
4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLIC ACID HYDRAZIDE 95.00%
5G
$ 1233.77

American Custom Chemicals Corporation
4,5,6,7-TETRAHYDRO-1H-INDAZOLE-3-CARBOXYLIC ACID HYDRAZIDE 95.00%
1G
$ 771.89

Total 5 raw suppliers

Chemical Property of 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Chemical Property:

Refractive Index:1.629
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：83.80000
Density:1.331g/cm³
LogP:0.98320
XLogP3:0.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:180.10111102
Heavy Atom Count:13
Complexity:208

Purity/Quality:

98%min ^*data from raw suppliers

4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC2=C(C1)C(=NN2)C(=O)NN

Technology Process of 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

There total 4 articles about 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 4492-02-8
ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carboxylate

: 90434-92-7
ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Guidance literature:: With hydrazine hydrate; In ethanol; for 36h; Reflux;
DOI:10.1111/j.1747-0285.2012.01365.x

Reference yield:

: 5396-14-5
ethyl 2-oxo-2-(2-oxocyclohexyl)acetate

: 90434-92-7
ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate; acetic acid / 0 °C / Reflux

2: hydrazine hydrate / ethanol / 36 h / Reflux

With hydrazine hydrate; acetic acid; In ethanol;
DOI:10.1111/j.1747-0285.2012.01365.x

Reference yield:

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 90434-92-7
ethyl 4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium ethanolate / ethanol / 7 h / 0 - 20 °C

2: hydrazine hydrate; acetic acid / 0 °C / Reflux

3: hydrazine hydrate / ethanol / 36 h / Reflux

With sodium ethanolate; hydrazine hydrate; acetic acid; In ethanol;
DOI:10.1111/j.1747-0285.2012.01365.x