196302-89-3

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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-, acetate
  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-, acetate
  3. CAS NO:196302-89-3
  4. Molecular Formula: C39H46 O7
  5. Molecular Weight: 626.78
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 196302-89-3.mol
  9. Article Data: 1

• 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-, acetate(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-, acetate(196302-89-3)
  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-, acetate(196302-89-3)

• 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: 196302-89-3(Hazardous Substances Data)

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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 ACETATE

  Cas No: 196302-89-3

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196302-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196302-89-3 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 196302-89:
(8*1)+(7*9)+(6*6)+(5*3)+(4*0)+(3*2)+(2*8)+(1*9)=153
153 % 10 = 3
So 196302-89-3 is a valid CAS Registry Number.

196302-89-3Upstream product

• 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 
• 98906-30-0 (+/-)-2,5,6-tri-O-benzyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 108-24-7 acetic anhydride 
• 196302-88-2 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 

196302-89-3Downstream Products

196302-89-3Relevant articles and documents

Versatile synthesis of myo-inositol phospholipid precursors

Grove, Simon J. A.,Gilbert, Ian H.,Holmes, Andrew B.,Painter, Gavin F.,Hill, Malcolm L.

, p. 1633 - 1634 (1997)

Homochiral myo-inositol derivatives 16 and 20 and their corresponding enantiomers possessing either the natural or unnatural ring stereochemistry for inositol phospholipids are synthesised from myo-inositol derivatives 8 and 9 respectively using camphor d

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