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33446-14-9

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33446-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33446-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,4 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33446-14:
(7*3)+(6*3)+(5*4)+(4*4)+(3*6)+(2*1)+(1*4)=99
99 % 10 = 9
So 33446-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-8-7-9(3-5-11(8)16-2)10(13)4-6-12(14)15/h3,5,7H,4,6H2,1-2H3,(H,14,15)

33446-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-methoxy-3-methylphenyl)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names 3-(4-Methoxy-3-methylbenzoyl)propionic 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:33446-14-9 SDS

33446-14-9Relevant articles and documents

New turn on fluorimetric sensor for direct detection of ultra-trace ferric ions in industrial wastewater and its application by test strips

Kamel, Rasha M.,El-Sakka, Sahar S.,Bahgat, Khaled,Monir, Marina R.,Soliman

, (2021)

New 5-(4-(dimethylamino)phenyl)-4-(2-(4-methoxy-3-methylphenyl)-2-oxoethyl)-1H-pyrazol-3(2 H)-one (AAP) sensor was synthesized and well characterized. AAP sensor was developed for direct detection of ultra-traces of Fe3+ ions in industrial wast

(+)- And (-)-mutisianthol: First total synthesis, absolute configuration, and antitumor activity

Bianco, Graziela G.,Ferraz, Helena M. C.,Costas, Arinice M.,Costa-Lotufo, Leticia V.,Pessoa, Claudia,De Moraes, Manoel O.,Schreins, Marcus G.,Pfaltz, Andreas,Silva Jr., Luiz F.

supporting information; scheme or table, p. 2561 - 2566 (2009/09/25)

The first synthesis of the natural product (+)-mutisianthol was accomplished in 11 steps and in 21% overall yield from 2-methylanisole. The synthesis of its enantiomer was also performed in a similar overall yield. The absolute configuration of the sesquiterpene (+)-mutisianthol was assigned as (15,37?). Key steps in the route are the asymmetric hydrogenation of a nonfunctionalized olefin using chiral iridium catalysts and the ring contraction of 1,2-dihydronaphthalenes using thallium(III) or iodine(III). The target molecules show moderate activity against the human tumor cell lines SF-295, HCT-8, and MDA-MB-435.

Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity

-

, (2008/06/13)

Compounds of the formula where the symbols are as defined in the specification, have retinoid agonist, antagonist or negative hormone-like biological activity.

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