Cas 188301-01-1,1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate]

188301-01-1

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Basic information

Product Name: 1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate]
Synonyms: 1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate]
CAS NO:188301-01-1
Molecular Formula:
Molecular Weight: 1393.36
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate](CAS DataBase Reference)
NIST Chemistry Reference: 1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate](188301-01-1)
EPA Substance Registry System: 1D-3,4,5-tri-O-propanoyl-myo-inositol-1,2,6-tris[bis(2-benzyloxyethyl)-phosphate](188301-01-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 188301-01-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 188301-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,3,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188301-01:
(8*1)+(7*8)+(6*8)+(5*3)+(4*0)+(3*1)+(2*0)+(1*1)=131
131 % 10 = 1
So 188301-01-1 is a valid CAS Registry Number.

188301-01-1Upstream product

54555-84-9 benzyl iodoethyl ether

188301-01-1Downstream Products

188301-01-1Relevant academic research and scientific papers

Analogues of 1D-MYO-inositol 1,2,6-trisphosphate. Preparation of carboxymethyl and 2-hydroxyethyl phosphate derivatives

Malmberg, Mats,Rehnberg, Nicola

, p. 109 - 112 (1997)

Acylation of 1D-myo-inositol 1,2,6-trisphosphate (α-trinositol) followed by alkylation of the phosphate groups with benzyl bromoacetate or 2-benzyloxyethyl iodide and deprotection provides a route to analogues with modified phosphate groups. The modificat

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