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5-TERT-BUTYL METHYLISOPHTHALATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,3-Benzenedicarboxylic acid, 5-(1,1-dimethylethyl)-, 1,3-dimethyl ester

    Cas No: 16308-65-9

  • USD $ 1.9-2.9 / Gram

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  • 16308-65-9 Structure
  • Basic information

    1. Product Name: 5-TERT-BUTYL METHYLISOPHTHALATE
    2. Synonyms: 5-TERT-BUTYLBENZENE-1,3-BIS-METHYL CARBOXYLATE;5-TERT-BUTYL METHYLISOPHTHALATE;METHYL 5-TERT-BUTYL-ISOPHTHALATE DIESTER;5-Tetr-butyl methylisophthalate;DIMETHYL 5-TERT-BUTYLISOPHTHALATE
    3. CAS NO:16308-65-9
    4. Molecular Formula: C14H18O4
    5. Molecular Weight: 250.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16308-65-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 334.6°C at 760 mmHg
    3. Flash Point: 160.2°C
    4. Appearance: /
    5. Density: 1.079g/cm3
    6. Vapor Pressure: 0.000126mmHg at 25°C
    7. Refractive Index: 1.499
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-TERT-BUTYL METHYLISOPHTHALATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-TERT-BUTYL METHYLISOPHTHALATE(16308-65-9)
    12. EPA Substance Registry System: 5-TERT-BUTYL METHYLISOPHTHALATE(16308-65-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16308-65-9(Hazardous Substances Data)

16308-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16308-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16308-65:
(7*1)+(6*6)+(5*3)+(4*0)+(3*8)+(2*6)+(1*5)=99
99 % 10 = 9
So 16308-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O4/c1-14(2,3)11-7-9(12(15)17-4)6-10(8-11)13(16)18-5/h6-8H,1-5H3

16308-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 5-tert-butylbenzene-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 5-tert-Butyl-isophthalsaeure-dimethylester

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:16308-65-9 SDS

16308-65-9Relevant articles and documents

SYNTHETIC METHODS PERTAINING TO TERT-BUTYL-BENZENE-BASED COMPOUNDS

-

Paragraph 0035; 0036; 0037; 0038, (2013/07/31)

According to some aspects, the present disclosure pertains to methods of forming dimethyl 5-tert-butylisophthalate which comprise comprising converting 5-tert-butylisophthalic acid into dimethyl 5-tert-butylisophthalate in synthesis procedures that compri

C3-Symmetric chiral trisimidazoline: The role of a third imidazoline and its application to the nitro Michael reaction and the α-amination of β-ketoesters

Murai, Kenichi,Fukushima, Shunsuke,Nakamura, Akira,Shimura, Masato,Fujioka, Hiromichi

experimental part, p. 4862 - 4868 (2011/08/03)

We describe the necessity of the C3-symmetry and the role of a third imidazoline of trisimidazoline 3, which was recently developed by us as a new entry of organocatalyst. The utility of 3 as a Br?nsted base catalyst in the nitro Michael reaction and the α-amination of β-ketoesters was shown, and the recyclability of the catalyst was also demonstrated.

BISAMIDE CYTOKINE INHIBITORS

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Page/Page column 110, (2008/06/13)

The present invention provides low molecular weight compounds useful as cytokine inhibitors, and compositions thereof. In particular, compounds of the invention are bisamides and are useful as anti-inflammatory agents. In one aspect the compounds have the

HETEROCYCLIC CYTOKINE INHIBITORS

-

Page/Page column 136, (2010/11/27)

The present invention provides low molecular weight compounds useful as cytokine inhibitors, and compositions thereof. In particular, compounds of the invention are useful as anti-inflammatory, anti-pain or anti-cancer agents. There are further provided m

Dimetalation: The acidity of monometalated arenes towards superbasic reagents

Baston, Eckhard,Maggi, Raimondo,Friedrich, Kirstin,Schlosser, Manfred

, p. 3985 - 3989 (2007/10/03)

Twofold hydrogen/metal interconversions ("dimetalations") can be accomplished with "spiny" arenes (tert-butylbenzene, 1,4-di-tert-butylbenzene, 1,1,3,3-tetramethylindane and congeners) and N,N-crowded anilines (2,2,6,6-tetramethyl-1-phenylpiperidine and N

Chemo- and regioselective cyclotrimerization of monoynes catalyzed by a nickel(0) and zinc(II) phenoxide system

Mori,Ikeda,Odashima

, p. 181 - 182 (2007/10/03)

A binary metal system of nickel(0) and zinc(II) phenoxide catalyzed the chemo- and regioselective cyclotrimerization of monoynes.

Synthesis of 2,5- and 2,4-cyclohexadiene-1,3-dicarboxylates via reductive alkylation of isophthalates

Seneci, Pierfausto,Caspani, Marco,Monti, Federica,Carrano, Lucia,Lociuro, Sergio,Ciabatti, Romeo

, p. 795 - 809 (2007/10/03)

Substituted 2,5-(structure 1) and 2,4-(structure 2) cyclohexadiene-1,3-dicarboxylates were prepared via Birch reductive alkylation of substituted isophthalates with alkylating agents such as alkyl and allyl halides, alkyl dihalides, α-halocarboxylates and expoxides. A brief discussion about their reactivity and stability is presented.

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