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3749-36-8

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3749-36-8 Usage

Description

3,4-Dihydro-2H-pyran-2-methanol, also known as dihydropyran-2-methanol, is an organic compound with the chemical formula C6H12O2. It is a colorless liquid at room temperature and is commonly used in various applications due to its unique chemical properties.

Uses

Used in Chemical Synthesis:
3,4-Dihydro-2H-pyran-2-methanol is used as a protecting group for alcohols in organic synthesis. It provides a mild and selective method for the immobilization and cleavage of alcohols, which is crucial in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,4-Dihydro-2H-pyran-2-methanol is used as a key intermediate in the synthesis of various drugs and drug candidates. Its ability to protect alcohol functional groups makes it a valuable tool in the development of new medications.
Used in Flavor and Fragrance Industry:
3,4-Dihydro-2H-pyran-2-methanol is also utilized in the flavor and fragrance industry as a building block for the creation of various scent compounds. Its unique chemical structure allows for the development of novel fragrances and flavors.
Used in Material Science:
In the field of material science, 3,4-Dihydro-2H-pyran-2-methanol is employed in the development of new polymers and materials with specific properties. Its versatility in chemical reactions enables the creation of materials with tailored characteristics for various applications.
Overall, 3,4-Dihydro-2H-pyran-2-methanol is a versatile compound with a wide range of applications across different industries, including chemical synthesis, pharmaceuticals, flavor and fragrance, and material science. Its unique chemical properties make it an essential tool in the development of new products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 3749-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3749-36:
(6*3)+(5*7)+(4*4)+(3*9)+(2*3)+(1*6)=108
108 % 10 = 8
So 3749-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c7-5-6-3-1-2-4-8-6/h2,4,6-7H,1,3,5H2

3749-36-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H56124)  3,4-Dihydro-2H-pyran-2-methanol, 96%   

  • 3749-36-8

  • 1g

  • 386.0CNY

  • Detail
  • Alfa Aesar

  • (H56124)  3,4-Dihydro-2H-pyran-2-methanol, 96%   

  • 3749-36-8

  • 5g

  • 1288.0CNY

  • Detail
  • Aldrich

  • (55665)  3,4-Dihydro-2H-pyran-2-methanol  ≥98.5% (GC)

  • 3749-36-8

  • 55665-5ML

  • 2,459.34CNY

  • Detail
  • Aldrich

  • (55665)  3,4-Dihydro-2H-pyran-2-methanol  ≥98.5% (GC)

  • 3749-36-8

  • 55665-25ML

  • 8,979.75CNY

  • Detail

3749-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dihydro-2H-pyran-2-methanol

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-3,4-dihydro-2H-pyran

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:3749-36-8 SDS

3749-36-8Relevant articles and documents

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Komada et al.

, p. 5,6 (1979)

-

Towards a library of chromene cannabinoids: A combinatorial approach on solid supports

Kapeller, Dagmar C.,Br?se, Stefan

supporting information; experimental part, p. 161 - 164 (2011/03/19)

A novel solid-phase synthesis towards classical cannabinoids is presented. Starting from immobilized salicylaldehydes the desired THC-analogous tricycles are obtained in four atom-economic steps including cleavage. The reagents of the employed reactions (domino oxa-Michael-aldol, Wittig, and Diels-Alder) can be varied easily, providing the basis for a combinatorial approach. Overall yields range from 20-60%. Georg Thieme Verlag Stuttgart New York.

Efficient polymer-assisted strategy for the deprotection of protected oligosaccharides

Tanaka, Hiroshi,Ishida, Tadasuke,Matoba, Nobuatsu,Tsukamoto, Hirokazu,Yamada, Haruo,Takahashi, Takashi

, p. 6349 - 6352 (2007/10/03)

(Chemical Equation Presented) New strategies in sugar synthesis: A prelinker containing a dihydropyranyl moiety and an activated ester can be attached to a sugar, which is then loaded onto an amino-modified support by amidation. Standard protecting-group manipulations are possible. Final cleavage of the linker under mildly acidic conditions provides the fully deprotected oligosaccharides. TFA=trifluoroacetic acid.

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