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Isobenzofuran, 1,3-dihydro-5-[(2-propynyloxy)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83469-16-3 Structure
  • Basic information

    1. Product Name: Isobenzofuran, 1,3-dihydro-5-[(2-propynyloxy)methyl]-
    2. Synonyms:
    3. CAS NO:83469-16-3
    4. Molecular Formula: C12H12O2
    5. Molecular Weight: 188.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83469-16-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Isobenzofuran, 1,3-dihydro-5-[(2-propynyloxy)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isobenzofuran, 1,3-dihydro-5-[(2-propynyloxy)methyl]-(83469-16-3)
    11. EPA Substance Registry System: Isobenzofuran, 1,3-dihydro-5-[(2-propynyloxy)methyl]-(83469-16-3)
  • 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: 83469-16-3(Hazardous Substances Data)

83469-16-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83469-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83469-16:
(7*8)+(6*3)+(5*4)+(4*6)+(3*9)+(2*1)+(1*6)=153
153 % 10 = 3
So 83469-16-3 is a valid CAS Registry Number.

83469-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(prop-2-ynoxymethyl)-1,3-dihydro-2-benzofuran

1.2 Other means of identification

Product number -
Other names 1,3-dihydro-2-benzofuran-5-ylmethyl 2-propynyl ether

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:83469-16-3 SDS

83469-16-3Downstream Products

83469-16-3Relevant articles and documents

Rhodium-catalyzed [2 + 2 + 2] cyclotrimerization in an aqueous-organic biphasic system

Kinoshita, Hidenori,Shinokubo, Hiroshi,Oshima, Koichiro

, p. 7784 - 7785 (2003)

Macrocyclization via rhodium-catalyzed intramolecular [2 + 2 + 2] annulation of triynes has been explored in an aqueous-organic biphasic system. The biphasic system controls the concentration of hydrophobic substrates in the aqueous reaction phase and offers diluted reaction conditions without the use of a slow addition technique. The system also achieves selective cross-annulation between hydrophobic diynes and hydrophilic alkynes. Copyright

A short synthetic route to a hybrid molecule benzosultine-sulfone via [2+2+2] cyclotrimerization using Mo(CO)6

Kotha, Sambasivarao,Sreevani, Gaddamedi

, p. 1204 - 1210 (2019/11/14)

Here, we report an improved and short synthetic route to benzosultine-sulfone via [2+2+2] cyclotrimerization as a key step, starting with dipropargyl ether and 1,4-dibromo-2-butyne with an overall yield of 16%.

Ruthenium-catalyzed cyclotrimerization of α-amino-α-propargyl carboxylates and phosphonates with 1,6-diynes: Synthesis of α-CF3-containing phenylalanine derivatives and their P-analogs

Zotova,Vasilyeva,Osipov

, p. 2455 - 2460 (2015/08/03)

Ruthenium-catalyzed cocyclotrimerization of α-amino-α-propargyl-α-trifluoromethyl carboxylates and phosphonates with functional 1,6-diynes gives the corresponding CF3-containing phenylalanine derivatives and their phosphorus analogs.

Ruthenium carbene mediated [2+2+2] cyclotrimerizations

Mallagaray, álvaro,Medina, Sandra,Domínguez, Gema,Pérez-Castells, Javier

supporting information; experimental part, p. 2114 - 2118 (2010/10/03)

Second-generation Grubbs catalyst and Hoveyda-Grubbs catalyst are able to catalyze both crossed [2+2+2] cyclotrimerization of diynes with alkynes and di- or trimerizations of diynes. Selection of the reaction conditions allows us to favor one particular p

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