196306-63-5

• 

• Basic information

  1. Product Name: myo-Inositol, 2,4-bis-O-(phenylmethyl)-5-O-2-propenyl-
  2. Synonyms: myo-Inositol, 2,4-bis-O-(phenylmethyl)-5-O-2-propenyl-
  3. CAS NO:196306-63-5
  4. Molecular Formula: C23H28 O6
  5. Molecular Weight: 400.46
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 196306-63-5.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: myo-Inositol, 2,4-bis-O-(phenylmethyl)-5-O-2-propenyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: myo-Inositol, 2,4-bis-O-(phenylmethyl)-5-O-2-propenyl-(196306-63-5)
  11. EPA Substance Registry System: myo-Inositol, 2,4-bis-O-(phenylmethyl)-5-O-2-propenyl-(196306-63-5)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 196306-63-5(Hazardous Substances Data)

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• 2,4-BIS-O-BENZYL-5-O-2-ALLYL-MYO-INOSITOL

  Cas No: 196306-63-5

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196306-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196306-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,3,0 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 196306-63:
(8*1)+(7*9)+(6*6)+(5*3)+(4*0)+(3*6)+(2*6)+(1*3)=155
155 % 10 = 5
So 196306-63-5 is a valid CAS Registry Number.

196306-63-5Upstream product

• 196302-92-8 1D-5-O-allyl-2,6-di-O-benzyl-3-O-endo,4-O-exo-(L-1',7',7'-trimethylbicyclo<2.2.1>hept-2'-ylidene)-myo-inositol 
• 100-39-0 benzyl bromide 
• 196302-84-8 (1R*,5R*,6R*,7S*,8S*,9R*)-8,9-bis(benzyloxy)-6-<(4'-methoxyphenyl)methoxy>-2,4-dioxabicyclo<3.3.1>nonan-7-ol 
• 125288-07-5 (1R*,3S*,5R*,6R*,7S*,8R*,9R*)-6-<(4'-methoxyphenyl)methoxy>-2,4,10-trioxatricyclo<3.3.1.1^3,7>decane-8,9-diol 
• 196302-87-1 (1R*,5R*,6S*,7S*,8R*,9R*)-6,9-bis(benzyloxy)-8-<(4'-methoxyphenyl)methoxy>-7-(prop-2'-enyl)-2,4-dioxabicyclo<3.3.1>nonane 

196306-63-5Downstream Products

196306-63-5Relevant articles and documents

Development of inositol-based antagonists for the d-myo-inositol 1,4,5-trisphosphate receptor

Keddie, Neil S.,Ye, Yulin,Aslam, Tashfeen,Luyten, Tomas,Bello, Davide,Garnham, Clive,Bultynck, Geert,Galione, Antony,Conway, Stuart J.

supporting information; experimental part, p. 242 - 244 (2011/03/20)

The syntheses of four d-myo-inositol 1,4,5-trisphosphate (InsP3) derivatives, incorporating phosphate bioisosteres at the 5-position, are reported. The methyl phosphate ester and sulfate derivatives retain InsP 3 receptor (InsP3

General synthesis of 3-phosphorylated mj'o-inositol phospholipids and derivatives

Painter, Gavin F.,Grove, Simon J. A.,Gilbert, Lan H.,Holmes, Andrew B.,Raithby, Paul R.,Hill, Malcolm L.,Hawking, Phillip T.,Stephens, Leonard R.

, p. 923 - 935 (2007/10/03)

The D-3-phosphorylated wyo-inositol phospholipids PtdIns(3)P, PtdIns(3,4)P2, PtdIns(3,4,5)P3 and PtdIns(3,5)P2 were synthesised from /yo-inositol orthoformate 8. Key transformations included the regioselective DIBAL- and trimethylaluminium-mediated cleavages of wiyo-inositol orthoformate intermediates and a resolution-protection protocol using the camphor acetals 17. The final reductive debenzylation was effected with Pearlman's catalyst [Pd(OH)J in the presence of sodium hydrogen carbonate. The biological properties of the phospholipids were evaluated against various protein kinases (PKB and PDK-1) in which they played an important activation role.

Synthesis of 3-Position-Modified Analogues of myo-Inositol 1,4,5-Trisphosphate, Tools for Investigation of the Polyphosphoinositide Pathway of Cellular Signaling

Liu, Changsheng,Potter, Barry V. L.

, p. 8335 - 8338 (2007/10/03)

Methods for the synthesis of 3-O-(carboxymethyl)- and 3-O-alkylated myo-inositol 1,4,5-trisphosphates in racemic form from myo-inositol have been devised. For DL-3-O-(carboxymethyl)-myo-inositol 1,4,5-trisphosphate, an analogue of myo-inositol 1,3,4,5-tet

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