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116409-38-2

Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116409-38-2 Structure

  • Basic information

    1. Product Name: Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol
    2. Synonyms: Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol;2H-Pyran-2-Methanol, tetrahydro-2,6-diMethyl-, (2R,6S)-rel-
    3. CAS NO:116409-38-2
    4. Molecular Formula: C8H16O2
    5. Molecular Weight: 144.21144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116409-38-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 193.727°C at 760 mmHg
    3. Flash Point: 65.818°C
    4. Appearance: /
    5. Density: 0.934g/cm3
    6. Vapor Pressure: 0.121mmHg at 25°C
    7. Refractive Index: 1.434
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol(116409-38-2)
    12. EPA Substance Registry System: Trans-Tetrahydro-2,6-dimethyl-2H-pyran-2-methanol(116409-38-2)

  • 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: 116409-38-2(Hazardous Substances Data)

116409-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116409-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,0 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116409-38:
(8*1)+(7*1)+(6*6)+(5*4)+(4*0)+(3*9)+(2*3)+(1*8)=112
112 % 10 = 2
So 116409-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-7-4-3-5-8(2,6-9)10-7/h7,9H,3-6H2,1-2H3/t7-,8+/m1/s1

116409-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,6S)-2,6-dimethyloxan-2-yl]methanol

1.2 Other means of identification

Product number -
Other names trans-2,6-dimethyl-2-hydroxymethyltetrahydropyran

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:116409-38-2 SDS

116409-38-2Downstream Products

116409-38-2Relevant articles and documents

Ketal-lactone compounds and their stereoselective cleavage to cyclic ethers

Jun, Jong-Gab,Lee, Dong Woo

, p. 8207 - 8210 (1997)

The easy preparation of ketal-lactone compounds via Diels-Alder reaction, followed by hydrolysis and cyclization and excellent stereoselective ring opening of the ketal-lactone to 6-membered and 7- membered cyclic ethers are described.

STEREOSELECTIVE REDUCTION OF BICYCLIC ACETALS. A METHOD FOR REDUCTIVE GENERATION OF HETEROCYCLIC RING SYSTEMS

Ishihara, Kazuaki,Mori, Atsunori,Yamamoto, Hisashi

, p. 6613 - 6616 (1987)

A new synthetic process for the construction of oxygen-containing heterocyclic systems starting from bicyclic acetals is described.

Diastereoselective Construction of 2,2,6-Trisubstituted Tetrahydropyrans by Intramolecular Alkylation Reaction of Lithiium Enolates Generated from α-Alkoxy Carboxylates

Fujisawa, Tamotsu,Okumura, Yoshiyuki,Morita, Kazuhisa,Ukaji, Yutaka

, p. 3487 - 3489 (2007/10/02)

The intramolecular alkylation reaction of enolates of t-butyl α-alkoxy carboxylates in THF-HMPA proceeded stereoselectively to afford 2,2,6-trisubstituted tetrahydropyrans with high cis-selectivity.

STEREOSELECTIVE REDUCTION OF ACETALS. A METHOD FOR REDUCTIVE GENERATION OF HETEROCYCLIC RING SYSTEMS

Ishihara, Kazuaki,Mori, Atsunori,Yamamoto, Hisashi

, p. 4595 - 4612 (2007/10/02)

A new synthetic process for the construction of oxygen-containing heterocyclic systems starting from bicyclic acetals is described.We have investigated the mechanism and the stereochemical course of the reductive cleavage of acetals.

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