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226889-57-2

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226889-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226889-57-2 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, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 226889-57:
(8*2)+(7*2)+(6*6)+(5*8)+(4*8)+(3*9)+(2*5)+(1*7)=182
182 % 10 = 2
So 226889-57-2 is a valid CAS Registry Number.

226889-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1D-2,4,5,6-tetra-O-benzyl-1-O-<(1'S)-camphanoyl>-3-O-(4'-methoxybenzyl)-myo-inositol

1.2 Other means of identification

Product number -
Other names (1S,4R)-4,7,7-Trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid (1S,2R,3S,4S,5R,6R)-2,3,4,6-tetrakis-benzyloxy-5-(4-methoxy-benzyloxy)-cyclohexyl ester

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:226889-57-2 SDS

226889-57-2Relevant 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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