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(+)-5,6-o-Cyclohexylidene-l-ascorbic acid is a chemical compound derived from l-ascorbic acid, also known as vitamin C. It possesses antioxidant properties and is commonly used in skincare products due to its ability to protect the skin from oxidative damage and promote collagen synthesis. The cyclohexylidene moiety in the compound enhances its stability and solubility, making it a more effective and stable form of vitamin C for topical use.
Used in Skincare Industry:
(+)-5,6-o-Cyclohexylidene-l-ascorbic acid is used as an antioxidant in skincare products for its ability to protect the skin from oxidative damage and promote collagen synthesis.
Used in Pharmaceutical Industry:
(+)-5,6-o-Cyclohexylidene-l-ascorbic acid is used as a potential anti-cancer and anti-inflammatory agent due to its potential medical applications.

6614-52-4

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6614-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6614-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6614-52:
(6*6)+(5*6)+(4*1)+(3*4)+(2*5)+(1*2)=94
94 % 10 = 4
So 6614-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O6/c13-8-9(14)11(15)17-10(8)7-6-16-12(18-7)4-2-1-3-5-12/h7,10,13-14H,1-6H2/t7?,10-/m1/s1

6614-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3S)-1,4-dioxaspiro[4.5]decan-3-yl]-3,4-dihydroxy-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 5,6-O-cyclohexylidene ascorbic 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:6614-52-4 SDS

6614-52-4Relevant academic research and scientific papers

REDOX POLYMERIZABLE COMPOSITION WITH PHOTOLABILE TRANSITION METAL COMPLEXES

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Page/Page column 54, (2017/05/19)

Polymerizable compositions comprising a redox initiator system is disclosed. The redox initiator system comprises a photolabile transition metal complex that photolyzes and initiates the redox cycle. Dental compositions comprising dental resins and the ph

REDOX POLYMERIZABLE DENTAL COMPOSITION WITH PHOTOLABILE TRANSITION METAL COMPLEXES

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Page/Page column 54, (2017/09/02)

Polymerizable dental compositions comprising a redox initiator system is disclosed. The redox initiator system comprises a photolabile transition metal complex that photolyzes and initiates the redox cycle.

REDOX POLYMERIZABLE COMPOSITION WITH PHOTOLABILE REDUCING AGENTS

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Page/Page column 55, (2017/09/02)

Polymerizable compositions comprising a redox initiator system is disclosed. The redox initiators comprises a photolabile reducing agent, that photolyzes and initiates the redox cycle. Dental compositions comprising dental resins and the photolabile redox initiator system are also described.

Total Synthesis of Symbioramide, a Novel Ca(2+)-ATPase Activator from Symbiodinium sp.

Yoshida, Jun,Nakagawa, Masako,Seki, Hiroko,Hino, Tohru

, p. 343 - 350 (2007/10/02)

The first total synthesis of symbioramide 1 has been accomplished by the coupling of D-erythro-dihydrosphingosine with an unusual, chiral α-hydroxy-β,γ-unsaturated fatty acid prepared from L-ascorbic acid, and simultaneously established the complete stereostructure of 1 to be (2S,2'R,3R,3'E)-N-(2'-hydroxyoctadec-3'-enoyl)dihydrosphingosine.

A New Convenient Method for the Synthesis of Chiral C3-Synthons

Emons, Carry H.H.,Kuster, Ben F.M.,Vekemans, Jozef A.J.M.,Sheldon, Roger A.

, p. 359 - 362 (2007/10/02)

Routes are described for the facile preparation of protected optically pure D- and L-glyceric acid (1a,b; 2a,b) starting from D-mannitol, D-isoascorbic acid and L-ascorbic acid.The key step is a ruthenium catalyzed oxidative cleavage of the vicinal diols 4a,b or the α-hydroxy acids 7a,b; 10a,b.

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