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16462-65-0

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16462-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16462-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,6 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16462-65:
(7*1)+(6*6)+(5*4)+(4*6)+(3*2)+(2*6)+(1*5)=110
110 % 10 = 0
So 16462-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H22O10/c1-29-14-6-10-9(5-12(14)22)16(8-3-13(23)18(25)15(4-8)30-2)20(28,19(26)27)11(7-21)17(10)24/h3-6,11,16-17,21-25,28H,7H2,1-2H3,(H,26,27)

16462-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name plicatic acid

1.2 Other means of identification

Product number -
Other names (1S)-1r-(3,4-dihydroxy-5-methoxy-phenyl)-2c,3t,7-trihydroxy-3c-hydroxymethyl-6-methoxy-1,2,3,4-tetrahydro-[2t]naphthoic acid

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:16462-65-0 SDS

16462-65-0Upstream product

16462-65-0Downstream Products

16462-65-0Relevant articles and documents

Asymmetric total synthesis of (-)-plicatic acid via a highly enantioselective and diastereoselective nucleophilic epoxidation of acyclic trisubstitued olefins

Sun, Bing-Feng,Hong, Ran,Kang, Yan-Biao,Deng, Li

supporting information; experimental part, p. 10384 - 10385 (2009/12/23)

(Chemical Equation Presented) The first total synthesis of (-)-plicatic acid has been achieved by a concise and enantioselective route. In this synthesis, a conceptually new strategy featuring an asymmetric epoxidation-intramolecular epoxy-ring-opening Friedel-Crafts reaction sequence was developed for the stereoselective construction of the 2,7′- cyclolignane skeleton bearing contiguous quaternary-quaternary-tertiary stereocenters. The implementation of this strategy was enabled by the development of a modified protocol for the Seebach epoxidation with TADOOH, which affords an unprecedented, highly enantioselective and diastereoselective epoxidation with a range of α-carbonyl-β-substituted acrylates 3.

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