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16691-59-1

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16691-59-1 Usage

Uses

Useful synthetic building block demonstrated by Tristan Lambert to enable access to chiral Br?nsted acid catalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 16691-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16691-59:
(7*1)+(6*6)+(5*6)+(4*9)+(3*1)+(2*5)+(1*9)=131
131 % 10 = 1
So 16691-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O10/c1-21-11(16)6-7(12(17)22-2)9(14(19)24-4)10(15(20)25-5)8(6)13(18)23-3/h6H,1-5H3

16691-59-1SDS

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 pentamethyl cyclopenta-1,3-diene-1,2,3,4,5-pentacarboxylate

1.2 Other means of identification

Product number -
Other names pentacarbomethoxycyclopentadiene

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:16691-59-1 SDS

16691-59-1Relevant articles and documents

Highly Enantioselective Synthesis of Cyclic Aminals with a Cyclopentadiene-Based Chiral Carboxylic Acid

Sui, Yuebo,Cui, Peng,Liu, Sensheng,Zhou, Yanmei,Du, Peng,Zhou, Haifeng

supporting information, p. 215 - 218 (2018/01/26)

A highly enantioselective aminalization of 2-aminobenzenesulfonamides and aldehydes catalyzed by a novel cyclopentadiene-based chiral carboxylic acid has been realized. The cost-effective and readily synthesized cyclopentadiene-based chiral carboxylic aci

Thermal Rearrangements and Reactions of 5-Alkyl-1,2,3,4,5-pentakis(methoxycarbonyl)cyclopentadienes

Jefferson, Elizabeth A.,Warkentin, John

, p. 463 - 467 (2007/10/02)

Studies of the thermal reactions of five 5-alkyl-1,2,3,4,5-pentakis(methoxycarbonyl)cyclopentadienes in methanol solvent are described, where the alkyl groups are benzhydryl, methoxymethyl, 1-adamantyl, p-methoxybenzyl, and benzyl.The benzyl cyclopentadiene system undergoes thermal -sigmatropic rearrangement via methoxycarbonyl migrations while the other cyclopentadienes undergo C-alkyl bond heterolysis to ion-pair intermediates, which are scavenged by solvent.First-order rate constants for solvolysis of the methoxymethyl, 1-adamantyl, and p-methoxymethyl systems in methanol solvent were determined and that for the benzhydryl system was estimated from a single measurement of the half-life.

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