1D-myo-inositol 1,2,4,5,6-pentakisphosphate

Base Information Edit

Chemical Name:1D-myo-inositol 1,2,4,5,6-pentakisphosphate
CAS No.:20298-94-6
Molecular Formula:C₆H₁₇O₂₁P₅
Molecular Weight:580.057
Hs Code.:
UNII:AY0A4IZV42
Nikkaji Number:J608.454K
Wikipedia:Inositol_pentakisphosphate
Wikidata:Q27101946
Metabolomics Workbench ID:50526
Mol file:20298-94-6.mol

Synonyms:myo-inositol 1,2,4,5,6-pentakisphosphate;AY0A4IZV42;1D-myo-inositol 1,2,4,5,6-pentakisphosphate;Inositol 1,2,4,5,6-pentaphosphate;Ins(1,2,4,5,6)P5;UNII-AY0A4IZV42;Myo-inositol 1,2,4,5,6-pentaphosphate;myo-Inositol 2,3,4,5,6-pentakisphosphate;DL-Myo-inositol 1,2,4,5,6-pentaphosphate;inositol 1,2,4,5,6-pentakisphosphate;Myo-inositol, 1,2,4,5,6-pentakis(dihydrogen phosphate);D-myo-inositol 1,2,4,5,6-pentakisphosphate;20298-94-6;1D-myo-inositol 1,2,4,5,6-pentakis(dihydrogen phosphate);20298-95-7;SCHEMBL2710469;CHEBI:16507;[(1R,2R,4R,5S)-3-hydroxy-2,4,5,6-tetraphosphonooxycyclohexyl] dihydrogen phosphate;PD053095;C04563;Q27101946;D-myo-Inositol 1,2,4,5,6-pentakis-phosphate, >=96% (HPLC)

Suppliers and Price of 1D-myo-inositol 1,2,4,5,6-pentakisphosphate

Supply Marketing:Edit

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 1D-myo-inositol 1,2,4,5,6-pentakisphosphate Edit

Chemical Property:

XLogP3:-9.2
Hydrogen Bond Donor Count:11
Hydrogen Bond Acceptor Count:21
Rotatable Bond Count:10
Exact Mass:579.89504254
Heavy Atom Count:32
Complexity:824

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)O
Isomeric SMILES:[C@@H]1([C@H](C([C@H]([C@@H](C1O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O

Technology Process of 1D-myo-inositol 1,2,4,5,6-pentakisphosphate

There total 2 articles about 1D-myo-inositol 1,2,4,5,6-pentakisphosphate 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:

: [3H]-Phytic acid

: 573-35-3,633-88-5,2831-74-5,4956-00-7,7336-80-3,13004-72-3,13331-65-2,15421-51-9,21667-10-7,26277-10-1,26545-79-9,34218-99-0,34219-00-6,34219-01-7,35275-50-4,46495-37-8,46495-38-9,46495-39-0,57652-30-9,69256-52-6,84414-08-4,111901-84-9
(+/-)-myo-Inositol-1-phosphate

: 20298-94-6,20298-95-7,20298-96-8,20298-97-9,23393-17-1,23486-93-3,25663-09-6,26326-85-2,26326-86-3,31662-65-4,40322-16-5,40322-17-6,114418-96-1,134176-37-7
(+/-)-myo-Inosit-1,2,3,4,5-pentakis-dihydrogenphosphat

: 41613-02-9,1311140-98-3
Inositol 1,2,3-triphosphate

: DL-myo-inositol 1,2-bis(phosphate)

Guidance literature:: With phytase from wheat bran of T_. aestivum L_. cv. Nourin No_. 61; water; In acetate buffer; at 37 ℃; pH=5.5; Product distribution;
DOI:10.1271/bbb.64.995