99782-78-2

Basic information

• Product Name: DL-1,4-BIS-O-(PHENYLMETHYL)-MYO INOSITOL
• Synonyms: DL-1,4-BIS-O-(PHENYLMETHYL)-MYO INOSITOL;UCJKCSNAJUPHIM-IPJCAIGPSA-N
• CAS NO: 99782-78-2
• Molecular Formula: C₂₀H₂₄O₆
• Molecular Weight: 362.42
• Mol File: 99782-78-2.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DL-1,4-BIS-O-(PHENYLMETHYL)-MYO INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: DL-1,4-BIS-O-(PHENYLMETHYL)-MYO INOSITOL(99782-78-2)
• EPA Substance Registry System: DL-1,4-BIS-O-(PHENYLMETHYL)-MYO INOSITOL(99782-78-2)

Safety Data

• Hazardous Substances Data: 99782-78-2(Hazardous Substances Data)

Upstream product

• 129662-36-8 (+/-)-1,4-Di-O-benzyl-2,3-di-O-(2-methoxyethoxymethyl)-chiro-inositol 
• 17793-95-2 (1RS,2RS)-cyclohexa-3,5-diene-1,2-diol 
• 100-39-0 benzyl bromide 
• 23393-20-6 (+/-)-3-O-benzyl-1,2:4,5-di-O,O-cyclohexylidene-myo-inositol 
• 98906-25-3 (±)-1,2-O-isopropylidene-3,6-di-O-benzyl-myo-inositol 
• 130659-80-2 (4S,5R,6S)-4-Hydroxy-5,6-bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-enone 
• 129662-34-6 (1S,4S,5R,6R)-5,6-Bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-ene-1,4-diol 
• 129662-35-7 C₂₈H₃₈O₈ 
• 130659-82-4 (5S,6S)-5,6-Bis-(2-methoxy-ethoxymethoxy)-cyclohex-2-ene-1,4-dione 
• 129662-34-6 (+/-)-1,2,4/3-2,3-Di-O-(2-methoxyethoxymethyl)cyclohex-5-ene-1,2,3,4-tetrol 
• 104826-13-3 1D-4,5-di-O-allyl-3,6-di-O-benzyl-1-l-menthoxyacetyl-myo-inositol 
• 104826-12-2 (+/-)-4,5-di-O-allyl-3,6-di-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 98925-52-1 (+/-)-5,6-di-O-allyl-1,4-di-O-benzyl-myo-inositol 
• 100-44-7 benzyl chloride 

Downstream Products

• 16749-94-3 (+/-)-2,3,4,5,6-penta-O-acetyl-1-O-benzyl-myo-inositol 
• 98906-25-3 (+/-)-1,4-di-O-benzyl-5,6-O-isopropylidine-myo-inositol 
• 1365626-51-2 L-(-)-5-acetyl-1,3,6-tri-O-benzyl-myo-inositol 
• 98906-30-0 (±)-1,3,6-tri-O-benzyl-myo-inositol 
• 501669-17-6 (±)-1,3,6-tri-O-benzyl-myo-inositol 
• 115184-71-9 (+/-)-1,3,4-tri-O-benzyl-myo-inositol 
• 131147-14-3 (+/-)-1,3,4,5-tetra-O-benzyl-myo-inositol 
• 142631-56-9 1,3,4,6-tetrakis-O-benzyl-myo-inositol 
• 5517-47-5 1⁽³⁾,2,4⁽⁶⁾,5,6⁽⁴⁾-penta-O-acetyl-sn-myo-inositol 
• 110298-84-5 (+/-)-myo-inositol 1,2,4,5-tetrakisphosphate 
• 114218-17-6 (+/-)-4,5-di-O-acetyl-1-O-allyl-2,3,6-tri-O-benzyl-myo-inositol 
• 114218-27-8 (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidene-myo-inosose-2 
• 114218-23-4 (+/-)-1-O-allyl-2,5-di-O-benzyl-3,4-O-isopropylidene-scyllo-inositol 
• 114218-20-1 (+/-)-2-O-allyl-1,4-di-O-benzyl-myo-inositol 

Relevant articles and documents

Design and synthesis of lipid-coupled inositol 1,2,3,4,5,6-hexakisphosphate derivatives exhibiting high-affinity binding for the HIV-1 MA domain

The precursor of Gag protein (Pr55Gag) of human immunodeficiency virus, the principal structural component required for virus assembly, is known to bind d-myo-phosphatidylinositol 4,5-bisphosphate (PIP2). The N-terminus of Pr55G

Tetrakisphosphates and Bispyrophosphates of myo-Inositol Derivatives as Allosteric Effectors of Human Hemoglobin: Synthesis, Molecular Recognition, and Oxygen Release

Various 2,5- and 1,4-substituted and unsubstituted myo-inositol tetrakisphosphates and bispyrophosphates were prepared following a general synthetic pathway. All final compounds were tested for their capability to induce oxygen release from human hemoglob

TOTAL SYNTHESIS OF chiro-INOSITOL 2,3,5-TRISPHOSPHATE: A myo-INOSITOL 1,4,5-TRISPHOSPHATE ANALOGUE FROM BENZENE VIA PHOTO-OXIDATION

The inositol tris- and tetrakis-phosphate analogues (4) and (14) have been synthesized from benzene by a sequence including reaction of singlet oxygen with a trans-cyclohexa-3,5-diene-1,2-diol (3) derivative.