1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name)

Base Information

Chemical Name:1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name)
CAS No.:20744-60-9
Molecular Formula:C33H25NO8
Molecular Weight:563.563
Hs Code.:

Synonyms:

Suppliers and Price of 1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name)

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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Total 5 raw suppliers

Chemical Property of 1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name)

Chemical Property:

Vapor Pressure:1.7E-21mmHg at 25°C
Boiling Point:735.5°C at 760 mmHg
Flash Point:306°C
Density:1.296g/cm³

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name)

There total 6 articles about 1-cyanobutane-1,2,3,4-tetrayl tetrabenzoate (non-preferred name) 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: 82.0%

: C₃₃H₂₇NO₉

: 20744-60-9
2,3,4,5-tetra-O-benzoyl-D-arabinononitrile

Guidance literature:: With pyridine; methanesulfonyl chloride; at -15 - 20 ℃; for 3h;
DOI:10.1016/j.tet.2014.02.035

Reference yield:

: D-arabinose diethyl dithioacetal

: 20744-60-9
2,3,4,5-tetra-O-benzoyl-D-arabinononitrile

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 48 h / 0 - 20 °C

2: mercury(II) oxide; mercury dichloride / water; acetone / 3.5 h / 20 °C

3: sodium acetate; hydroxylamine hydrochloride / ethanol / 2 h / 20 °C

4: pyridine; methanesulfonyl chloride / 3 h / -15 - 20 °C

With pyridine; hydroxylamine hydrochloride; sodium acetate; methanesulfonyl chloride; mercury dichloride; mercury(II) oxide; In ethanol; water; acetone;
DOI:10.1016/j.tet.2014.02.035

Reference yield:

: 103476-14-8,17013-95-5
2,3,4,5-tetra-O-benzoyl-D-arabinose diethyl dithioacetal

: 20744-60-9
2,3,4,5-tetra-O-benzoyl-D-arabinononitrile

Guidance literature:: Multi-step reaction with 3 steps

1: mercury(II) oxide; mercury dichloride / water; acetone / 3.5 h / 20 °C

2: sodium acetate; hydroxylamine hydrochloride / ethanol / 2 h / 20 °C

3: pyridine; methanesulfonyl chloride / 3 h / -15 - 20 °C

With pyridine; hydroxylamine hydrochloride; sodium acetate; methanesulfonyl chloride; mercury dichloride; mercury(II) oxide; In ethanol; water; acetone;
DOI:10.1016/j.tet.2014.02.035