2-Furanacetonitrile, a-hydroxy-

Base Information

Chemical Name:2-Furanacetonitrile, a-hydroxy-
CAS No.:932-29-6
Molecular Formula:C6H5NO2
Molecular Weight:123.111
Hs Code.:

Synonyms:

Suppliers and Price of 2-Furanacetonitrile, a-hydroxy-

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
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price

Total 1 raw suppliers

Chemical Property of 2-Furanacetonitrile, a-hydroxy-

Chemical Property:

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-Furanacetonitrile, a-hydroxy-

There total 2 articles about 2-Furanacetonitrile, a-hydroxy- 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:

: 98-01-1
furfural

: 613-90-1
benzoyl cyanide

: 932-29-6
2-furyl-2-hydroxyacetonitrile

: 86352-16-1
2-(Furan-2-yl)-2-hydroxy-1-phenylethanone

: 134-81-6
benzil

Guidance literature:: With titanium(III) chloride; potassium carbonate; acetic acid; Yield given. Multistep reaction. Yields of byproduct given; 1) water, 2 h, r.t., 2) t-BuOH, 35 deg C, 4 h;
DOI:10.1021/jo00062a038

Reference yield:

: 98-01-1
furfural

: 74-90-8
hydrogen cyanide

: 932-29-6
2-furyl-2-hydroxyacetonitrile

: 10017-07-9
(S)-2-(2'-furyl)-2-hydroxy-acetonitrile

: 121986-08-1
(R)-(-)-2-(2-furyl)-2-hydroxyacetonitrile

Guidance literature:: With phosphate buffer; 2-hydroxy-1,2,3-propanetricarboxylate; Aqua Gel matrix; hydroxynitrile lyase from Prunus amygdalus (EC 4.1.2.10); In di-isopropyl ether; at 20 ℃; for 72h; pH=5.0; Further Variations:; Reagents; single phase reaction, without support, reaction time; Kinetics; Product distribution;
DOI:10.1002/adsc.200606139