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185430-32-4

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185430-32-4 Usage

Furanone ring

The compound contains a furanone ring, which is a five-membered heterocyclic ring with an oxygen atom and a carbonyl group (C=O).

Hydroxy group

The compound has a hydroxy group (-OH) attached to the furanone ring, which can form hydrogen bonds and participate in various chemical reactions.

Hexadecyl chain

The compound has a long hexadecyl chain (a 16-carbon alkyl chain) with a carbonyl group (C=O) at one end, which can provide hydrophobic and lipophilic properties.

Triphenylmethoxy methyl group

The compound contains a triphenylmethoxy methyl group (a methyl group attached to a triphenylmethoxy group), which can provide steric hindrance and influence the compound's reactivity and physical properties.

Chiral molecule

The compound is a chiral molecule, meaning it has a specific three-dimensional arrangement of atoms and can exist in different enantiomeric forms.

(5R) designation

The compound has a specific stereochemistry, denoted by the (5R) designation, which indicates the configuration of the carbon atom at position 5 in the furanone ring.

Potential applications

The compound has potential applications in various fields, including pharmaceuticals, materials science, and organic chemistry research, but further investigation and synthesis are needed to determine its specific properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 185430-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,3 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 185430-32:
(8*1)+(7*8)+(6*5)+(5*4)+(4*3)+(3*0)+(2*3)+(1*2)=134
134 % 10 = 4
So 185430-32-4 is a valid CAS Registry Number.

185430-32-4SDS

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 (R)-3-hexadecanoyl-5-(triphenylmethoxymethyl)tetronic acid

1.2 Other means of identification

Product number -
Other names (R)-3-Hexadecanoyl-4-hydroxy-5-trityloxymethyl-5H-furan-2-one

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:185430-32-4 SDS

185430-32-4Relevant articles and documents

Solution-phase and solid-phase syntheses of enzyme inhibitor RK-682 and antibiotic agglomerins

Schobert, Rainer,Jagusch, Garsten

, p. 6129 - 6132 (2007/10/03)

The enzyme inhibitor RK-682 (5A)-(+)-1 was prepared in solution and on a solid support from (2R)-glycerates in five steps and ca. 40% overall yield. Key steps were a ring-closing tandem addition-Wittig alkenation reaction of the respective protected or im

Asymmetric synthesis of RK-682 and its analogs, and evaluation of their protein phosphatase inhibitory activities

Sodeoka, Mikiko,Sampe, Ruriko,Kagamizono, Terumi,Osada, Hiroyuki

, p. 8775 - 8778 (2007/10/03)

We report an asymmetric synthesis of a potent tyrosine phosphatase inhibitor, RK-682 and its analogs. The absolute stereochemistry of RK-682 was determined to be (R). The inhibitory activities of RK-682 and its analogs, (R)-1a, (S)-1a, (R)-1b and (R)-1c toward various protein phosphatases (VHR, cdc25A, cdc25B, and PPI) are also reported.

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