131435-04-6

Basic information

• Product Name: (1α,2β,3α,4α,5α,6β)-6-fluoro-1,2,3,4,5-cyclohexanepentol 1,2,5-trisphosphate
• CAS NO: 131435-04-6
• Molecular Weight: 422.088
• Mol File: 131435-04-6.mol

Chemical Properties

• CAS DataBase Reference: (1α,2β,3α,4α,5α,6β)-6-fluoro-1,2,3,4,5-cyclohexanepentol 1,2,5-trisphosphate(CAS DataBase Reference)
• NIST Chemistry Reference: (1α,2β,3α,4α,5α,6β)-6-fluoro-1,2,3,4,5-cyclohexanepentol 1,2,5-trisphosphate(131435-04-6)
• EPA Substance Registry System: (1α,2β,3α,4α,5α,6β)-6-fluoro-1,2,3,4,5-cyclohexanepentol 1,2,5-trisphosphate(131435-04-6)

Safety Data

• Hazardous Substances Data: 131435-04-6(Hazardous Substances Data)

Upstream product

• 118993-51-4 (3aα,4α,5β,6β,7β,7aα)-4,5-bis(benzyloxy)-6,7-epoxyhexahydro-2,2-dimethylbenzo-1,3-dioxole 
• 125291-06-7 (3aα,4β,5α,6β,7α,7aα)-6,7-bis(benzyloxy)-5-fluorohexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4-ol 
• 130633-23-7 (3aα,4α,5β,6α,7β,7aα)-6-fluorohexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol 
• 125291-08-9 (3aα,4α,5β,6α,7β,7aα)-6-fluorohexahydro-2,2-dimethylbenzo-1,3(2H)-dioxol-4,5,7-triol tris(dibenzylphosphate) 
• 917-54-4 methyllithium 

Relevant articles and documents

Rapid synthesis and properties of (±)-6-deoxy-6-fluoro-myo-inositol- 1,4,5-tris(phosphate) an analogue of myo-inositol-1,4,5-tris(phosphate)

(±)-6-Deoxy-6-fluoro-myo-inositol-1,4,5-tris(phosphate) was prepared from myoinositol derivatives. Its affinity for the Endoplasmic Reticulum receptors was interpreted using 31P-NMR studies.

Synthesis, acid-base behavior, and binding properties of 6-modified myo- inositol 1,4,5-tris(phosphate)s

myo-Inositol 1,4,5-tris(phosphate) was modified at position 6. The analogues synthesized are reported in this publication are 6-deoxy-myo- inositol 1,4,5-tris(phosphate), 6-fluoro-6-deoxy-myo-inositol 1,4,5- tris(phosphate), epi-inositol 1,4,5-tris(phosph

MICROBIAL OXIDATION IN SYNTHESIS: PREPARATION OF MYO-INOSITOL PHOSPHATES AND RELATED CYCLITOL DERIVATIVES FROM BENZENE.

Pseudomonas putida oxidation of benzene affords cis-3,5-cyclohexadiene-1,2-diol (2) which is used as a novel precursor for the synthesis of D- and L-myo-inositol 1,4,5-triphosphates, (-)-(1) and (+)-(1).The versatility of this approach to functionalised cyclitols is illustrated in the synthesis of myo-inositol 1-phosphate (19), 6-deoxy, 6-deoxy-6-fluoro, and 6-deoxy-6-methyl myo-inositols (31), (37) and (43), and their 1,4,5-trisphosphate derivatives (33), (39) and (45).

MICROBIAL OXIDATION IN SYNTHESIS: PREPARATION OF 6-DEOXY CYCLITOL ANALOGUES OF MYO-INOSITOL 1,4,5-TRIPHOSPHATE FROM BENZENE

The novel 6-deoxy, 6-deoxy-6-fluoro and 6-deoxy-6-methyl myo-inositol 1,4,5-triphosphate derivatives (4), (5) and (6) were derived from benzene via microbial oxidation to cis -1,2-dihydroxycyclohexa-3,5-diene (2) and conversion through to the key epoxyace