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(3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98167-08-9 Structure
  • Basic information

    1. Product Name: (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid
    2. Synonyms: (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid
    3. CAS NO:98167-08-9
    4. Molecular Formula:
    5. Molecular Weight: 300.265
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98167-08-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid(98167-08-9)
    11. EPA Substance Registry System: (3R,4S,5R)-3,4,5-triacetoxycyclohex-1-ene-1-carboxylic acid(98167-08-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 98167-08-9(Hazardous Substances Data)

98167-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98167-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98167-08:
(7*9)+(6*8)+(5*1)+(4*6)+(3*7)+(2*0)+(1*8)=169
169 % 10 = 9
So 98167-08-9 is a valid CAS Registry Number.

98167-08-9Relevant articles and documents

Protection of COOH and OH groups in acid, base and salt free reactions

Zhu, Xiaotao,Qian, Bo,Wei, Rongbiao,Huang, Jian-Dong,Bao, Hongli

, p. 1444 - 1447 (2018)

We report an iron-catalyzed general functional group protection method with inexpensive reagents. This environmentally benign process does not use acids or bases, and does not produce waste products. Further purification beyond filtration and evaporation is, in most cases, unnecessary. Free COOH and OH groups can be protected in a one-pot reaction.

ACTIVE AGENTS AND METHODS OF THEIR USE FOR THE TREATMENT OF METABOLIC DISORDERS AND NONALCOHOLIC FATTY LIVER DISEASE

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Page/Page column 67; 88, (2019/12/28)

Disclosed herein are active agents, compositions containing them, unit dosage forms containing them, and methods of their use, e.g., for treating a metabolic disorder or nonalcoholic fatty liver disease or for modulating a metabolic marker or nonalcoholic fatty liver disease marker.

ACYLATED ACTIVE AGENTS AND METHODS OF THEIR USE FOR THE TREATMENT OF AUTOIMMUNE DISORDERS

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Page/Page column 156, (2019/12/28)

Disclosed herein are acylated active agents (e.g., acylated catechin polyphenols, acylated carotenoids, acylated mesalamines, acylated sugars, acylated shikimic acids, acylated ellagic acid, acylated ellagic acid analogue, and acylated hydroxybenzoic acids), active agent combinations (e.g., with a second agent that is a fatty acid) and methods of their use, e.g., for modulating an autoimmunity marker or for treating an autoimmune disorder.

New aspects of the Hunsdiecker-Barton halodecarboxylation-syntheses of phospha-shikimic acid and derivatives

Carbain, Benoit,Hitchcock, Peter B.,Streicher, Hansj?rg

supporting information; experimental part, p. 2717 - 2719 (2010/07/06)

We report an efficient synthetic approach to phospha-isosteres of important intermediates of the shikimic acid pathway by the application of the Hunsdiecker-Barton halodecarboxylation to cyclohexenylcarboxylic acids. As examples, phospha-shikimic acid, it

Cationic amphiphile with shikimic acid headgroup shows more systemic promise than its mannosyl analogue as DNA vaccine carrier in dendritic cell based genetic immunization

Srinivas, Ramishetti,Karmali, Priya P.,Pramanik, Dipankar,Garu, Arup,Mahidhar, Yenugonda Venkata,Majeti, Bharat K.,Ramakrishna, Sistla,Srinivas, Gunda,Chaudhuri, Arabinda

supporting information; experimental part, p. 1387 - 1391 (2010/09/05)

Mannosylated cationic vectors have been previously used for delivering DNA vaccines to antigen presenting cells (APCs) via mannose receptors expressed on the cell surface of APCs. Here we show that cationic amphiphiles containing mannose-mimicking quinic

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