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Benzoic acid 2-thienyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16693-98-4 Structure
  • Basic information

    1. Product Name: Benzoic acid 2-thienyl ester
    2. Synonyms: Benzoic acid 2-thienyl ester;Thiophen-2-ol benzoate
    3. CAS NO:16693-98-4
    4. Molecular Formula: C11H8O2S
    5. Molecular Weight: 204.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16693-98-4.mol
  • Chemical Properties

    1. Melting Point: 43-44 °C
    2. Boiling Point: 323.2±15.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.258±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoic acid 2-thienyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid 2-thienyl ester(16693-98-4)
    11. EPA Substance Registry System: Benzoic acid 2-thienyl ester(16693-98-4)
  • 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: 16693-98-4(Hazardous Substances Data)

16693-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16693-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16693-98:
(7*1)+(6*6)+(5*6)+(4*9)+(3*3)+(2*9)+(1*8)=144
144 % 10 = 4
So 16693-98-4 is a valid CAS Registry Number.

16693-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name thiophen-2-yl benzoate

1.2 Other means of identification

Product number -
Other names benzoic acid-[2]thienyl ester

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:16693-98-4 SDS

16693-98-4Relevant articles and documents

Visible-light-triggered direct benzoyloxylation of electron-rich arenes at room temperature without chelation assistance

Rao, Honghua,Wang, Ping,Li, Chao-Jun

supporting information, p. 6503 - 6507 (2013/01/15)

A RuII photocatalytic method was developed for the direct mono-benzoyloxylation of electron-rich aromatic and heteroaromatic systems even with an excess amount of benzoyl peroxide. The reaction was conducted at room temperature under visible light. The direct ArC-H benzoyloxylations occur without the assistance of any directing groups and can also tolerate various functional groups that have already shown diverse reactivities in transition-metal catalysis.

Synthesis of Five-membered 2-Heteroaryl 2-Heteroaromatic Carboxylates and Attempted Cyclization to Bisheteroaryl[2,3-b:3′2′-d]pyran-2-one

Lee, Chang Kiu,Yu, Ji Sook,Kim, Sun Hee

, p. 835 - 841 (2007/10/03)

2-Heteroaryl 2-heteroaromatic carboxylates were prepared by reactions of 2-heteroaromatic carbonyl chlorides and 2(5H)-furanone, 2(5H)-thiophenone, and 1-methyl-2(5H)-pyrrolone in triethylamine. The 1H nmr spectra of the esters showed that the electronic effect of both heteroaromatic rings did not cause any sizable shift from each other except for 1-methyl-2-pyrrolyl 1-methyl-2-pyrrolecarboxylate (5c). Attempts to cyclize the esters to heteroaryl-fused pyran-2-ones were unsuccessful. The results may be explained by the most stable conformation of the esters in which two heteroatoms are anti along the C-O bond of the ester group.

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