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1,2-Benzenedicarboxylic acid, 4-(hydroxymethyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

170433-63-3

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170433-63-3 Usage

Molecular weight

194.18 g/mol

Appearance

Colorless, odorless solid

Solubility

Soluble in organic solvents

Primary use

Precursor for the synthesis of polyethylene terephthalate (PET)

Applications

Production of plastic bottles, food containers, and synthetic fibers

Synthesis method

Esterification of terephthalic acid with methanol

Byproduct

Produced during the oxidation of p-xylene to terephthalic acid

Role

Crucial in the production of various polyester materials used in everyday products and applications

Check Digit Verification of cas no

The CAS Registry Mumber 170433-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,4,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 170433-63:
(8*1)+(7*7)+(6*0)+(5*4)+(4*3)+(3*3)+(2*6)+(1*3)=113
113 % 10 = 3
So 170433-63-3 is a valid CAS Registry Number.

170433-63-3Relevant academic research and scientific papers

The d10 route to dye-sensitized solar cells: Step-wise assembly of zinc(ii) photosensitizers on TiO2 surfaces

Bozic-Weber, Biljana,Constable, Edwin C.,Hostettler, Nik,Housecroft, Catherine E.,Schmitt, Ralf,Schoenhofer, Ewald

supporting information; experimental part, p. 5727 - 5729 (2012/07/27)

Dye-sensitized solar cells have been assembled using a sequential approach: a TiO2 surface was functionalized with an anchoring ligand, followed by metallation with Zn(OAc)2 or ZnCl2, and subsequent capping with a chromophore functionalized 2,2′:6′,2″- terpyridine; the DSCs exhibit surprisingly good efficiencies confirming the effectiveness of the new strategy for zinc-based DSC fabrication.

Vitamin D analogues

-

Page column 12, (2010/02/09)

The present invention relates to novel triaromatic compounds having the general formula (I): as well as to a method for preparing them and to their use in pharmaceutical compositions intended for use in human or veterinary medicine (in dermatology, in car

Triaromatic vitamin D analogues

-

, (2008/06/13)

The invention relates, as novel and useful industrial products, to triaromatic compounds, which are vitamin D analogues, of general formula (I): and also to a method for preparing them and to their use in pharmaceutical compositions intended for use in human or veterinary medicine, or alternatively in cosmetic compositions.

Cyclic amic acid derivatives

-

, (2008/06/13)

PCT No. PCT/JP97/00303 Sec. 371 Date Aug. 4, 1998 Sec. 102(e) Date Aug. 4, 1998 PCT Filed Feb. 7, 1997 PCT Pub. No. WO97/29078 PCT Pub. Date Aug. 14, 1997The present invention relates to a compound of the formula (I), or its pharmaceutically acceptable salt or ester: wherein Ar1 is an aryl group or a heteroaromatic ring group; Ar is a group of the formula each of Ar2 and Ar3 is an aryl group or a heteroaromatic ring group; Cy is an aryl group, a heteroaromatic ring group or an aliphatic ring group which may contain one or two oxygen atoms; A1 is a C1-4 chain hydrocarbon group; m is an integer of from 1 to 6; each of n and p is an integer of from 0 to 3; Q1 is a single bond, a group of the formula -CH2O-, -OCH2-, -CH2S- or -SCH2-, or a C1-6 chain hydrocarbon group; Q2 is a single bond or a group of the formula -(CH2)m- or -(CH2)n-W-(CH2)p-; Q3 is a single bond, an oxygen atom, a sulfur atom, a methylene group, a vinylene group or a group of the formula -CO-, -NH-, -COO-, -OCO-, -CH2CH2-, -OCH2-, -SCH2-, -CH2O-, -CH2S-, -NHCO- or -CONH-; R1 is a lower alkyl group; each of R2 and R3 is a hydrogen atom, a hydroxyl group or a lower alkyl group; W is an oxygen atom, a sulfur atom, a vinylene group or an ethynylene group; x is an integer of from 0 to 2; and y is 0 or 1; and an antitumor agent containing it as an active ingredient and intermediates for the production thereof.

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