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172323-66-9

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172323-66-9 Usage

Description

(2S)-3,6-dihydro-2H-pyran-2-ylmethanol is an organic compound with the chemical formula C6H10O2. It is a colorless liquid at room temperature and is derived from the organic compound 2H-pyran. Its structure consists of a six-membered oxygen-containing ring with a methanol group attached to it.

Uses

Used in Pharmaceutical Industry:
(2S)-3,6-dihydro-2H-pyran-2-ylmethanol is used as a building block in organic synthesis for the production of various pharmaceuticals and fine chemicals. Its stability and unique ring structure make it a valuable compound in the field of organic chemistry.
Used in Organic Synthesis:
(2S)-3,6-dihydro-2H-pyran-2-ylmethanol is used as a reagent in chemical reactions due to its stability and unique ring structure. It plays a crucial role in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 172323-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,3,2 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 172323-66:
(8*1)+(7*7)+(6*2)+(5*3)+(4*2)+(3*3)+(2*6)+(1*6)=119
119 % 10 = 9
So 172323-66-9 is a valid CAS Registry Number.

172323-66-9SDS

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 [(2S)-3,6-dihydro-2H-pyran-2-yl]methanol

1.2 Other means of identification

Product number -
Other names -

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:172323-66-9 SDS

172323-66-9Relevant articles and documents

Diastereoselective Reaction of Buta-1,3-diene with Chiral Derivatives of Glyoxylic Acid: Effective Route to Optically Pure 2-Substituted 3,6-Dihydro2H-pyrans

Kosior, Magorzata,Asztemborska, Monika,Jurczak, Janusz

, p. 87 - 91 (2004)

The influence of Lewis acids on the diastereoselectivity of [4+2] cycloaddition of buta-1,3-diene (4) to N-glyoxyloyl-(2R)-bornane- 10,2-sultam (6a) and (R)-8-phenylmenthyl glyoxylate (6b) was investigated and found to have high levels of asymmetric induc

Highly diastereoselective hetero-Diels-Alder reaction of buta-1,3-diene with N-glyoxyloyl-(2R)-bornane-10,2-sultam: An efficient synthesis of homochiral (S)-3-[2-{(methylsulfonyl)oxy}ethoxy]-4-(triphenylmethoxy)-1-butanol methanesulfonate

Kosior, Malgorzata,Malinowska, Malgorzata,Jozwik, Julita,Caille, Jean-Claude,Jurczak, Janusz

, p. 239 - 244 (2007/10/03)

The influence of Lewis acid on the diastereoselectivity of [4+2] cycloaddition of buta-1,3-diene to N-glyoxyloyl-(2R)-bornane-10,2-sultam was investigated and high levels of asymmetric induction were achieved. (S)-3-[2-{(Methylsulfonyl)oxy}ethoxy]-4-(trip

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