beta-d-Psicopyranose

Base Information

Chemical Name:beta-d-Psicopyranose
CAS No.:40461-85-6
Molecular Formula:
Molecular Weight:180.158
Hs Code.:
UNII:FT0PW5OPP0
Nikkaji Number:J3.047.017F
Mol file:40461-85-6.mol

Synonyms:beta-d-psicopyranose;FT0PW5OPP0;UNII-FT0PW5OPP0;40461-85-6;beta-psicose;.BETA.-D-PSICOPYRANOSE;SCHEMBL8828916

Suppliers and Price of beta-d-Psicopyranose

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 beta-d-Psicopyranose

Chemical Property:

XLogP3:-2.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:180.06338810
Heavy Atom Count:12
Complexity:162

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(C(C(C(O1)(CO)O)O)O)O
Isomeric SMILES:C1[C@H]([C@H]([C@H]([C@](O1)(CO)O)O)O)O

Technology Process of beta-d-Psicopyranose

There total 1 articles about beta-d-Psicopyranose 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:

: 1113-60-6
3-hydroxy-2-oxopropionic acid

: 533-49-3
L-erythrose

: 16354-64-6,18875-34-8
(3S,4S,5S)-1,3,4,5,6-pentahydroxyhexan-2-one

: 38029-84-4
α-D-psico-2.6-pyranose

: 40461-85-6
β-D-psico-2.6-pyranose

Guidance literature:: 3-hydroxy-2-oxopropionic acid; With magnesium(II) chloride hexahydrate; pyridoxal 5'-phosphate; transketolase from geobacillus stearothermophilus; thiamine diphosphate; In water; at 60 ℃; for 0.333333h; pH=7; Enzymatic reaction;

L-erythrose; With L-serin; sodium hydroxide; In water; at 60 ℃; for 96h; pH=7; Overall yield = 51 percent; Overall yield = 92 mg;
DOI:10.1002/cctc.201901756