Skip to Content
Merck
CN

55665

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

≥98.5% (GC)

Synonym(s):

2-Hydroxymethyl-3,4-dihydro-2H-pyran, 3,4-Dihydro-2H-pyran-2-ylmethanol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C6H10O2
CAS Number:
3749-36-8
Molecular Weight:
114.14
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
57651546
EC Number:
223-150-0
Beilstein/REAXYS Number:
107275
MDL number:
MFCD00051507
Assay:
≥98.5% (GC)

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

XMICBFRKICBBKD-UHFFFAOYSA-N

InChI

1S/C6H10O2/c7-5-6-3-1-2-4-8-6/h2,4,6-7H,1,3,5H2

SMILES string

OCC1CCC=CO1

assay

≥98.5% (GC)

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.478 (lit.), n20/D 1.479

bp

92-93 °C/25 mmHg (lit.)

density

1.101 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

100

Related Categories

Other Notes

Preparation of supported dihydropyran for mild immobilization and cleavage of alcohols

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

192.2 °F - closed cup

flash_point_c

89 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH1911
BCBW8715
BCBW3390
BCBN2279V
BCBL7232V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Preparation of supported dihydropyran for mild immobilization and cleavage of alcohols.
L.A. Thompson et al.
Tetrahedron Letters, 35, 9333-9333 (1994)
Facile Preparation of 2,6-Disubstituted Purines Using Solid-Phase Chemistry.
David A. Nugiel et al.
The Journal of organic chemistry, 62(1), 201-203 (1997-01-10)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service