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1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 315216-27-4 Structure
  • Basic information

    1. Product Name: 1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI)
    2. Synonyms: 1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI)
    3. CAS NO:315216-27-4
    4. Molecular Formula: C6H12O4
    5. Molecular Weight: 148.15708
    6. EINECS: N/A
    7. Product Categories: ALCOHOL
    8. Mol File: 315216-27-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI)(315216-27-4)
    11. EPA Substance Registry System: 1,3-Dioxane-4-methanol, 5-hydroxy-2-methyl-, (4R,5S)- (9CI)(315216-27-4)
  • 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: 315216-27-4(Hazardous Substances Data)

315216-27-4 Usage

Classification

Cyclic ether alcohol

Derivative of

Dioxane

Enantiomeric forms

(4R,5S) and (4S,5R)

Specific enantiomer

(4R,5S)(9CI)

Use as a solvent

Chemical reactions

Use as a stabilizer

Cosmetics and personal care products

Potential applications

Pharmaceuticals and drug synthesis

Health hazards

May pose health risks if not used properly or exposed to in high concentrations

Handling precautions

Handle with caution due to potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 315216-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,2,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 315216-27:
(8*3)+(7*1)+(6*5)+(5*2)+(4*1)+(3*6)+(2*2)+(1*7)=104
104 % 10 = 4
So 315216-27-4 is a valid CAS Registry Number.

315216-27-4SDS

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 2,4-O-ethylidene-L-erythritol

1.2 Other means of identification

Product number -
Other names (4R,5S)-4-Hydroxymethyl-2-methyl-[1,3]dioxan-5-ol

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:315216-27-4 SDS

315216-27-4Upstream product

315216-27-4Relevant articles and documents

Allelochemicals of the tropical weed Sphenoclea zeylanica

Hirai, Nobuhiro,Sakashita, Sou-ichi,Sano, Tadachika,Inoue, Toshiki,Ohigashi, Hajime,Premasthira, Cha-Um,Asakawa, Yukio,Harada, Jiro,Fujii, Yoshiharu

, p. 131 - 140 (2007/10/03)

Nine plant growth inhibitors were isolated from the tropical weed Sphenoclea zeylanica, which shows allelopathic properties. Those compounds hitherto not reported from any plant source were the isomers of cyclic thiosulfinate, (1S,3R,4R)-(+)- and (1R,3R,4R)-(-)-4-hydroxy-3-hydroxymethyl-1,2-dithiolane-1-oxides, and (2R,3R,4R)-(-)- and (2S,3R,4R)-(+)-4-hydroxy-3-hydroxymethyl-1,2-dithiolane-2-oxides. These were named Zeylanoxide A, epi-zeylanoxide A, zeylanoxide B and epi-zeylanoxide B, respectively. The absolute configurations at C-3 and C-4 were elucidated by chemical synthesis of both enantiomers from L- and D-glucose. Two of the inhibitors were secologanic acid and secologanoside, and three other inhibitors were by known secoiridoid glucosides formed as artifacts during extraction with methanol. The cyclic thiosulfinates and secoiridoid glucosides completely inhibit the root growth of rice seedlings at 3.0 mM. While the specific activity of the inhibitors was not high, since they accumulated to circa 0.61% S. zeylanica by dry weight, this suggests that the inhibitors are nervertheless potent allelochemicals in this weed. (C) 2000 Elsevier Science Ltd.

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