196302-88-2

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• Basic information

  1. Product Name: D-myo-Inositol, 2,4,5-tris-O-(phenylmethyl)-1,6-O-(1R,2R,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-
  2. Synonyms: D-myo-Inositol, 2,4,5-tris-O-(phenylmethyl)-1,6-O-(1R,2R,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-
  3. CAS NO:196302-88-2
  4. Molecular Formula: C₃₇H₄₄O₆
  5. Molecular Weight: 584.74
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 196302-88-2.mol
  9. Article Data: 2

• 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: D-myo-Inositol, 2,4,5-tris-O-(phenylmethyl)-1,6-O-(1R,2R,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-(CAS DataBase Reference)
  10. NIST Chemistry Reference: D-myo-Inositol, 2,4,5-tris-O-(phenylmethyl)-1,6-O-(1R,2R,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-(196302-88-2)
  11. EPA Substance Registry System: D-myo-Inositol, 2,4,5-tris-O-(phenylmethyl)-1,6-O-(1R,2R,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-(196302-88-2)

• 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: 196302-88-2(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 2,4,5-TRIS-O-BENZYL-1,6-O-[(124R)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPT-2-YLIDENE]-D-MYO-INOSITOL

  Cas No: 196302-88-2

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196302-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196302-88-2 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 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 196302-88:
(8*1)+(7*9)+(6*6)+(5*3)+(4*0)+(3*2)+(2*8)+(1*8)=152
152 % 10 = 2
So 196302-88-2 is a valid CAS Registry Number.

196302-88-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	1D-2,4,5-tri-O-benzyl-1-O-endo,6-O-exo-(D-1',7',7'-trimethylbicyclo<2.2.1>hept-2'-ylidene)-myo-inositol

1.2 Other means of identification

Product number	-
Other names	-

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:196302-88-2 SDS

196302-88-2Upstream product

• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 98906-30-0 (+/-)-2,5,6-tri-O-benzyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 196302-86-0 (1R*,5R*,6R*,7S*,8S*,9R*)-7,8,9-tris(benzyloxy)-6-<(4'-methoxyphenyl)methoxy>-2,4-dioxabicyclo<3.3.1>nonane 
• 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 

196302-88-2Downstream Products

• 226889-48-1 (1S,2S,3R,4S,5S,6S)-3,4,6-Tris-benzyloxy-5-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol 
• 114419-08-8 (+)-1L-2,5,6-tri-O-benzyl-myo-inositol 
• 196302-89-3 C₃₉H₄₆O₇ 

196302-88-2Relevant articles and documents

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.

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