tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate

Base Information

Chemical Name:tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate
CAS No.:88767-24-2
Molecular Formula:C₈H₁₄N₂O₂
Molecular Weight:170.211
Hs Code.:
DSSTox Substance ID:DTXSID90549054

Synonyms:88767-24-2;tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate;DTXSID90549054

Suppliers and Price of tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate

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

Total 1 raw suppliers

Chemical Property of tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:170.105527694
Heavy Atom Count:12
Complexity:216

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)C1=NNCC1

Technology Process of tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate

There total 1 articles about tert-Butyl 4,5-dihydro-1H-pyrazole-3-carboxylate 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:

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 1663-39-4,25232-27-3
tert-Butyl acrylate

: 501-53-1,94274-21-2
benzyl chloroformate

: 88767-24-2
t-butyl 4,5-dihydropyrazole-3-carboxylate

: 111709-24-1
3-(1,1-dimethylethyl) 1-(phenylmethyl) 1,3-pyrazolidinedicarboxylate

Guidance literature:: With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; Yield given. Multistep reaction. Yields of byproduct given; 1.) diethyl ether, 2 min; 2.) ethanol; 3.) ethyl acetate, water, 2 h;