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D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-

    Cas No: 226889-48-1

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  • 226889-48-1 Structure
  • Basic information

    1. Product Name: D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-
    2. Synonyms: D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-
    3. CAS NO:226889-48-1
    4. Molecular Formula: C35H38O7
    5. Molecular Weight: 570.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 226889-48-1.mol
  • 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, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-(226889-48-1)
    11. EPA Substance Registry System: D-myo-Inositol, 3-O-(4-methoxyphenyl)methyl-2,4,5-tris-O-(phenylmethyl)-(226889-48-1)
  • 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: 226889-48-1(Hazardous Substances Data)

226889-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226889-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,8,8 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 226889-48:
(8*2)+(7*2)+(6*6)+(5*8)+(4*8)+(3*9)+(2*4)+(1*8)=181
181 % 10 = 1
So 226889-48-1 is a valid CAS Registry Number.

226889-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,3R,4S,5S,6S)-3,4,6-Tris-benzyloxy-5-(4-methoxy-benzyloxy)-cyclohexane-1,2-diol

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:226889-48-1 SDS

226889-48-1Relevant 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.

The preparation of racemic and enantiomerically pure myo-inositol derivatives as intermediates for the synthesis of phosphatidylinositol 3-, 3,4-bis-, and 3,4,5-tris-phosphates and for the synthesis of analogues of 1D-myo-inositol 1,3,4,5-tetrakisphosphat

Desai, Trupti,Gigg, Jill,Gigg, Roy,Martin-Zamora, Eloisa

, p. 97 - 133 (2007/10/03)

Details of the products obtained by the tin-mediated allylation and benzylation of 1,2-O-isopropylidene-myo-inositol, which were previously described in a preliminary communication, are provided here. Some of the products from these reactions, particularl

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