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5S-IODO-1S,6S-3,7-DIOXABICYCLO[4,3,0]-NONAN-8-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87614-56-0

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87614-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87614-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,1 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87614-56:
(7*8)+(6*7)+(5*6)+(4*1)+(3*4)+(2*5)+(1*6)=160
160 % 10 = 0
So 87614-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H9IO3/c8-5-3-10-2-4-1-6(9)11-7(4)5/h4-5,7H,1-3H2/t4?,5-,7-/m0/s1

87614-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5S-iodo-1S,6S-3,7-dioxabicyclo<4,3,0>nonan-8-one

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:87614-56-0 SDS

87614-56-0Relevant academic research and scientific papers

ENANTIOSPECIFIC TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS FROM ARABINOSE

Fleet, G. W. J.,Gough, M. J.,Shing, T. K. M.

, p. 3661 - 3664 (2007/10/02)

The enantiospecific synthesis of pseudomonic acids from arabinose is described.

ENANTIOSPECIFIC SYNTHESES OF INTERMEDIATES IN THE TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS

Fleet, G. W. J.,Gough, M. J.

, p. 4509 - 4512 (2007/10/02)

Enantiospecific syntheses of 1S,6S-3,7-dioxabicyclonon-4-en-8-one (1) and of the enantiomer (2) from D- and L-arabinose respectively have been achieved by two different routes.The conversion of (1) to 6S-(3R-acetanilido)-3,6-dihydro-2H-pyranyl-N,N-dimethylacetamide (3), a key intermediate in the synthesis of pseudomonic acids, is described.

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