Welcome to LookChem.com Sign In|Join Free
  • or
CHROMAN-3-CARBOXYLIC ACID METHYL ESTER, also known as 3-Methoxycarbonylchroman, is a chemical compound with the molecular formula C10H10O3. It is a methyl ester derivative of chroman-3-carboxylic acid and is commonly used in the pharmaceutical industry as a building block for the synthesis of various biologically active molecules. CHROMAN-3-CARBOXYLIC ACID METHYL ESTER has been studied for its potential antioxidant and anti-inflammatory properties, making it a potential candidate for drug development. It is also used in the production of fragrances and flavors due to its pleasant aroma and taste. CHROMAN-3-CARBOXYLIC ACID METHYL ESTER is typically stored and handled in accordance with standard chemical safety procedures due to its potential reactivity and toxicity.

68281-60-7

Post Buying Request

68281-60-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

68281-60-7 Usage

Uses

Used in Pharmaceutical Industry:
CHROMAN-3-CARBOXYLIC ACID METHYL ESTER is used as a building block for the synthesis of various biologically active molecules for drug development.
Used in Antioxidant and Anti-Inflammatory Applications:
CHROMAN-3-CARBOXYLIC ACID METHYL ESTER is used as a potential candidate for drug development due to its antioxidant and anti-inflammatory properties.
Used in Fragrance and Flavor Production:
CHROMAN-3-CARBOXYLIC ACID METHYL ESTER is used as a component in the production of fragrances and flavors due to its pleasant aroma and taste.

Check Digit Verification of cas no

The CAS Registry Mumber 68281-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,8 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 68281-60:
(7*6)+(6*8)+(5*2)+(4*8)+(3*1)+(2*6)+(1*0)=147
147 % 10 = 7
So 68281-60-7 is a valid CAS Registry Number.

68281-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,4-dihydro-2H-chromene-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl chroman-3-carboxylate

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:68281-60-7 SDS

68281-60-7Downstream Products

68281-60-7Relevant academic research and scientific papers

Systematic methodology for the development of biocatalytic hydrogen-borrowing cascades: Application to the synthesis of chiral α-substituted carboxylic acids from α-substituted α,β-unsaturated aldehydes

Knaus, Tanja,Mutti, Francesco G.,Humphreys, Luke D.,Turner, Nicholas J.,Scrutton, Nigel S.

supporting information, p. 223 - 233 (2015/02/19)

Ene-reductases (ERs) are flavin dependent enzymes that catalyze the asymmetric reduction of activated carbon-carbon double bonds. In particular, α,β-unsaturated carbonyl compounds (e.g. enals and enones) as well as nitroalkenes are rapidly reduced. Conversely, α,β-unsaturated esters are poorly accepted substrates whereas free carboxylic acids are not converted at all. The only exceptions are α,β-unsaturated diacids, diesters as well as esters bearing an electron-withdrawing group in α- or β-position. Here, we present an alternative approach that has a general applicability for directly obtaining diverse chiral α-substituted carboxylic acids. This approach combines two enzyme classes, namely ERs and aldehyde dehydrogenases (Ald-DHs), in a concurrent reductive-oxidative biocatalytic cascade. This strategy has several advantages as the starting material is an α-substituted α,β-unsaturated aldehyde, a class of compounds extremely reactive for the reduction of the alkene moiety. Furthermore no external hydride source from a sacrificial substrate (e.g. glucose, formate) is required since the hydride for the first reductive step is liberated in the second oxidative step. Such a process is defined as a hydrogen-borrowing cascade. This methodology has wide applicability as it was successfully applied to the synthesis of chiral substituted hydrocinnamic acids, aliphatic acids, heterocycles and even acetylated amino acids with elevated yield, chemo- and stereo-selectivity. A systematic methodology for optimizing the hydrogen-borrowing two-enzyme synthesis of α-chiral substituted carboxylic acids was developed. This systematic methodology has general applicability for the development of diverse hydrogen-borrowing processes that possess the highest atom efficiency and the lowest environmental impact. This journal is

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 68281-60-7