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1,2-Benzenedicarboxylic acid, 4,5-dichloro-, monomethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145303-69-1

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145303-69-1 Usage

Chemical structure

1,2-Benzenedicarboxylic acid, 4,5-dichloro-, monomethyl ester

Physical state

Clear and colorless liquid

Odor

Faint, fruity

Usage

Raw material for polymer production

Polymers produced

Polyethylene terephthalate (PET)

Applications

Plastic bottles, containers, polyester fibers, and films

Safety

Relatively safe for use

Potential hazard

Irritation to the respiratory system at high concentrations

Precautions

Proper handling and storage required to ensure safety and prevent hazards

Check Digit Verification of cas no

The CAS Registry Mumber 145303-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,0 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145303-69:
(8*1)+(7*4)+(6*5)+(5*3)+(4*0)+(3*3)+(2*6)+(1*9)=111
111 % 10 = 1
So 145303-69-1 is a valid CAS Registry Number.

145303-69-1SDS

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 4,5-dichloro-2-methoxycarbonylbenzoate

1.2 Other means of identification

Product number -
Other names 4,5-dichloro-2-methoxycarbonyl benzoic 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:145303-69-1 SDS

145303-69-1Relevant academic research and scientific papers

Anthranilic sulfonamide CCK1/CCK2 dual receptor antagonists II: Tuning of receptor selectivity and in vivo efficacy

Pippel, Marna,Boyce, Kristen,Venkatesan, Hariharan,Phuong, Victor K.,Yan, Wen,Barrett, Terrance D.,Lagaud, Guy,Li, Lina,Morton, Magda F.,Prendergast, Clodagh,Wu, Xiaodong,Shankley, Nigel P.,Rabinowitz, Michael H.

, p. 6376 - 6378 (2009)

In the previous article we demonstrated how certain CCK2R-selective anthranilic amides could be structurally modified to afford high-affinity, selective CCK1R activity. We now describe our efforts at modulating and optimizing the CCK1R and CCK2R affinitie

N-SUBSTITUTED-5-SUBSTITUTED PHTHALAMIC ACIDS AS SORTILIN INHIBITORS

-

Page/Page column 51, (2015/02/06)

The present invention is directed to N-substituted-5-substituted phthalamic acids which of formula (A). The compounds are considered useful for the treatment of diseases treatment of a neurodegenerative disease, psychiatric disease, motorneuron disease, peripheral neuropathies, pain, neuroinflammation or atherosclerosis such as Alzheimer's disease and Parkinson's disease.

Protecting-group-free synthesis of a dual CCK1/CCK2 receptor antagonist

Liu, Jing,Deng, Xiaohu,Fitzgerald, Anne E.,Sales, Zachary S.,Venkatesan, Hariharan,Mani, Neelakandha S.

scheme or table, p. 2654 - 2660 (2011/05/08)

In our pursuit of an efficient, protecting-group-free synthesis of the dual CCK1/CCK2 receptor antagonist 1, we have developed chemoselective conditions for sulfonamide formation reaction in pure water and a PhNMe2 mediated carboxamide formatio

MODULATORS OF 5-HT RECEPTORS AND METHODS OF USE THEREOF

-

Page/Page column 138, (2010/12/18)

The present application relates to aryl- and heteroaryl-fused decahydropyrroloazepine, octahydrooxepinopyrrole, octahydropyrrolothiazepine dioxide, decahydrocyclohepta[c]pyrrole, and octahydrocyclohepta[c]pyrrole derivatives of formula (I), wherein R1,R2, R3, R4, R5, A, Y1, Y2, and Y3 are as defined in the specification. The present application also relates to compositions comprising such compounds, processes for making such compounds, and methods of treating disease conditions using such compounds and compositions, and methods for identifying such compounds.

SULFONAMIDE COMPOUNDS

-

Page/Page column 19, (2010/10/20)

Certain sulfonamide compounds are dual CCK1/CCK2 inhibitors useful in the treatment of CCK1/CCK2 mediated diseases.

Quinoxaline compounds

-

Page/Page column 15, (2008/06/13)

Certain amidophenyl-sulfonylamino-quinoxaline compounds are CCK2 modulators useful in the treatment of CCK2 mediated diseases.

COMPOUNDS HAVING ACTIVITY AT 5HT2C RECEPTOR AND USES THEREOF

-

Page 19, (2010/02/09)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed: wherein R1 is halogen, cyano, C1-6alkyl, C3-7cycloalkyl, C3-7cycloalkyloxy, C1-6alkoxy, C1 6alkylthio, hydroxy, amino, mono or di C1 6alkylamino, an N-linked 4 to 7 memb

Condensed pyridazinyl guanidines, their production and use

-

, (2008/06/13)

Pyridazinyl guanidines of the formula: wherein ring A is a benzene ring or a nitrogen-containing 6-membered aromatic ring, each of which may be substituted; and R1is an aromatic ring group which may be substituted, or a salt thereof, which have activity for inhibiting Na-H exchange and are useful as a prophylactic/therapeutic agent for ischemic cardiovascular diseases such as myocardial infarction and arrythmia.

ANGIOTENSIN II ANTAGONISTS INCORPORATING A SUBSTITUTED INDOLE OR DIHYDROINDOLE

-

, (2008/06/13)

Substituted heterocycles attached through a methylene bridge to novel substituted indole or dihydroindole derivative of the Formula I are useful as angiotensin II antagonists. STR1

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