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13417-49-7

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13417-49-7 Usage

Uses

5,6-Dihydro-2H-pyran-3-carboxaldehyde is a useful synthetic intermediate and a derivative of acrolein (A191200); a compound well-known for its use in the synthesis of acrylic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 13417-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,1 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13417-49:
(7*1)+(6*3)+(5*4)+(4*1)+(3*7)+(2*4)+(1*9)=87
87 % 10 = 7
So 13417-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O2/c7-4-6-2-1-3-8-5-6/h2,4H,1,3,5H2

13417-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-Dihydro-2H-pyran-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3,6-dihydro-2H-pyran-5-carbaldehyde

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:13417-49-7 SDS

13417-49-7Relevant articles and documents

COMPOUNDS AND METHODS OF TREATING OCULAR DISORDERS

-

Paragraph 00259, (2016/06/14)

A method of treating an ocular disorder in a subject associated with increased all-trans-retinal in an ocular tissue includes administering to the subject a therapeutically effective amount of a primary amine compound of formula (I); and pharmaceutically acceptable salts thereof.

The enantioselective hydrogenation of 5,6-dihydro-2H-pyran-3-carboxylic acid over a cinchona alkaloid-modified palladium catalyst: Asymmetric synthesis of a cockroach attractant

Szori, Kornel,Szollosi, Gyoergy,Bartok, Mihaly

scheme or table, p. 1354 - 1358 (2009/02/04)

A novel application of a cinchona-modified supported Pd catalyst is presented. The key step in the asymmetric synthesis of the cockroach attractant methyl (+)-tetrahydro-2H-pyran-3-carboxylate was the enantioselective hydrogenation of 5,6-dihydro-2H-pyran

Derivatives of 5,6-Dihydro-2H-pyran-3-carboxylic acid

Spreitzer, Helmut,Mueller, Petra,Buchbauer, Gerhard

, p. 963 - 970 (2007/10/02)

Some derivatives of 5,6-dihydro-2H-pyran-3-carboxaldehyde (7) and of its oxidation product 5,6-dihydro-2H-pyran-3-carboxylic acid (8) have been prepared.The aldehyde derivatives as well as the amides and esters of 8 have been tested in an insecticidal/fun

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