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2-Furancarboxylic acid, 3-[[4-(carboxymethyl)phenoxy]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61727-72-8

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61727-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61727-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61727-72:
(7*6)+(6*1)+(5*7)+(4*2)+(3*7)+(2*7)+(1*2)=128
128 % 10 = 8
So 61727-72-8 is a valid CAS Registry Number.

61727-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[4-(carboxymethyl)phenoxy]methyl]furan-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-(2-Carboxy-3-furylmethoxy)phenylessigsaeure

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:61727-72-8 SDS

61727-72-8Upstream product

61727-72-8Downstream Products

61727-72-8Relevant academic research and scientific papers

Dibenz[b,e]oxepinalkanoic acids as nonsteroidal antiinflammatory agents. 2. Dihydro 10 oxofuro and thieno[3,2 c] [1]benzoxepin 8 acetic acids

Aultz,McFadden,Lassman

, p. 456 - 458 (1977)

4,10 Dihydro-10-oxofuro[3,2-c][1]benzoxepin-8-acetic acid and 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetic acid were evaluated in the carrageenan paw edema assay with the thieno analogue being ten times more active than the furano compound and 1.3 times more active than indomethacin. The therapeutic ratio (antiinflammatory activity/gastric irritation liability) of the thieno analogue was 25 times that of indomethacin.

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