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5,6-dimethyl-4-oxo-pyran-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92490-75-0

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92490-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92490-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,9 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92490-75:
(7*9)+(6*2)+(5*4)+(4*9)+(3*0)+(2*7)+(1*5)=150
150 % 10 = 0
So 92490-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4/c1-4-5(2)12-7(8(10)11)3-6(4)9/h3H,1-2H3,(H,10,11)/p-1

92490-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethyl-4-oxopyran-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-4-pyrone-6-carboxylic acid

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:92490-75-0 SDS

92490-75-0Downstream Products

92490-75-0Relevant academic research and scientific papers

NITROGEN-CONTAINING HETEROCYCLIC COMPOUND

-

Paragraph 0333, (2017/08/01)

The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity and useful as a medicament such as a prophylactic or therapeutic drug for Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies and the like, and the like. The present invention relates to a compound represented by the formula (I) or a salt thereof. wherein each symbol is as described in the attached DESCRIPTION.

Photoisomerization of 4-Hydroxypyrylium Cations in Concentrated Sulfuric Acid

Pavlik, James W.,Patten, Arthur D.,Bolin, David R.,Bradford, Kenneth C.,Clennan, Edward L.

, p. 4523 - 4531 (2007/10/02)

Irradiation of di-, tri-, and tetraalkyl-4-hydroxypyrylium cations in concentrated sulfuric acid leads to the formation of 2-hydroxypyrylium cations as phototransposition products and, in certain cases, to furyl cations by a photo-ring-contraction reaction.Product analysis by spectroscopic techniques, deuterium labeling, and unambiguous synthesis reveals that 2-hydroxypyrylium cations are formed by two distinct transposition patterns and accordingly, by two distinct mechanistic pathways.The bond-forming and -breaking requirements of the major transposition pattern, which constitutes approximately 95percent of the reaction, are consistent with a mechanism initiated by 2,6-bridging in the first excited state of the 4-hydroxypyrylium cation.Similarly, the bond-formation and -breaking requirements of the minor pattern are consistent with a mechanism involving 2,5-bridging in the first excited state of the starting cation.

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