1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Base Information

Chemical Name:1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate
CAS No.:143366-63-6
Molecular Formula:C₁₀H₂₂NO₁₆P₃
Molecular Weight:505.203
Hs Code.:

Synonyms:1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Suppliers and Price of 1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

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 0 raw suppliers

Chemical Property of 1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

There total 4 articles about 1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate 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: 98.0%

: 136598-00-0
1-<3-Aminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

: 77287-34-4,77287-35-5,60100-09-6
formamide

: 143366-63-6
1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Guidance literature:: With methanol; sodium hydroxide; at 25 ℃; for 72h;
DOI:10.1016/S0008-6215(00)90513-5

Reference yield:

: 143366-60-3,143396-71-8
2,3,6-Tri-O-benzoyl-1-O-(tetrahydro-2-pyranyl)-D-myo-inositol

: 143366-63-6
1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Guidance literature:: Multi-step reaction with 6 steps

1: 1) 1H-tetrazole, 2) m-chloroperoxybenzoic acid / 1) CH₂Cl₂, 25 deg C, 8 h, 2) -78 deg C to 25 deg C, overnight

2: 88percent HCOOH, H₂O / tetrahydrofuran / 0.5 h / 25 °C

3: 1) 1H-tetrazole, 2) m-chloroperoxybenzoic acid / 1) CH₂Cl₂, 25 deg C, 1 h, 2) -78 deg C to 25 deg C, overnight

4: H₂ / Pd(OH)2-C / acetic acid / 6 h / 760 Torr

5: 63 percent / 0.8 M NaOH / 18 h / 25 °C

6: 98 percent / 1percent NaOH, MeOH / 72 h / 25 °C

With 1H-tetrazole; methanol; sodium hydroxide; formic acid; water; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium hydroxide - carbon; In tetrahydrofuran; acetic acid;
DOI:10.1016/S0008-6215(00)90513-5

Reference yield:

: 143366-59-0,143442-23-3,143442-24-4,143442-25-5
2,3,6-Tri-O-benzoyl-4,5-di-O-benzyl-1-O-(tetrahydro-2-pyranyl)-D-myo-inositol

: 143366-63-6
1-O-<3-Formylaminopropoxy(hydroxy)phosphinyl>-D-myo-inositol 4,5-bisphosphate

Guidance literature:: Multi-step reaction with 7 steps

1: H₂ / Pd(OH)2-C / aq. ethanol / 18 h / 760 Torr

2: 1) 1H-tetrazole, 2) m-chloroperoxybenzoic acid / 1) CH₂Cl₂, 25 deg C, 8 h, 2) -78 deg C to 25 deg C, overnight

3: 88percent HCOOH, H₂O / tetrahydrofuran / 0.5 h / 25 °C

4: 1) 1H-tetrazole, 2) m-chloroperoxybenzoic acid / 1) CH₂Cl₂, 25 deg C, 1 h, 2) -78 deg C to 25 deg C, overnight

5: H₂ / Pd(OH)2-C / acetic acid / 6 h / 760 Torr

6: 63 percent / 0.8 M NaOH / 18 h / 25 °C

7: 98 percent / 1percent NaOH, MeOH / 72 h / 25 °C

With 1H-tetrazole; methanol; sodium hydroxide; formic acid; water; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium hydroxide - carbon; In tetrahydrofuran; ethanol; acetic acid;
DOI:10.1016/S0008-6215(00)90513-5