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62417-02-1

Benzaldehyde, 2,4-bis[(3-methyl-2-butenyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62417-02-1 Structure

  • Basic information

    1. Product Name: Benzaldehyde, 2,4-bis[(3-methyl-2-butenyl)oxy]-
    2. Synonyms: 2,4-diprenyloxybenzaldehyde;
    3. CAS NO:62417-02-1
    4. Molecular Formula: C17H22O3
    5. Molecular Weight: 274.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62417-02-1.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: Benzaldehyde, 2,4-bis[(3-methyl-2-butenyl)oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzaldehyde, 2,4-bis[(3-methyl-2-butenyl)oxy]-(62417-02-1)
    11. EPA Substance Registry System: Benzaldehyde, 2,4-bis[(3-methyl-2-butenyl)oxy]-(62417-02-1)

  • 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: 62417-02-1(Hazardous Substances Data)

62417-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62417-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,1 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62417-02:
(7*6)+(6*2)+(5*4)+(4*1)+(3*7)+(2*0)+(1*2)=101
101 % 10 = 1
So 62417-02-1 is a valid CAS Registry Number.

62417-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis(3-methylbut-2-enoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 2,4-diprenyloxybenzaldehyde

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:62417-02-1 SDS

62417-02-1Relevant articles and documents

Highly efficient and selective deprotection method for prenyl, geranyl, and phytyl ethers and esters using borontrifluoride-etherate

Narender,Venkateswarlu,Madhur,Reddy, K. Papi

, p. 26 - 33 (2012/10/30)

An efficient, simple, and practical method has been developed for the deprotection of prenyl, geranyl, and phytyl ethers and esters of aromatic and aliphatic compounds using borontrifluoride-etherate (BF3· OEt2) at room temperature in good to excellent yields for the first time. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file. Copyright Taylor & Francis Group, LLC.

Synthesis of the naturally occurring prenylated coumarins balsamiferone and cedrelopsin by domino reactions

Patre, Rupesh E.,Parameswaran, Perunninakulath S.,Tilvea, Santosh G.

experimental part, p. 68 - 76 (2011/06/19)

Regioselective one step synthesis of naturally occurring prenyl coumarin balsamiferone is described using domino Wittig reaction, 3,3-sigmatropic rearrangements and deprenylation, while regioselective synthesis of cedrelopsin is described via domino Witti

Cascade wittig reaction-double claisen and cope rearrangements: One-pot synthesis of diprenylated coumarins gravelliferone, balsamiferone, and 6,8-diprenylumbelliferone

Patre, Rupesh E.,Shet, Jyoti B.,Parameswaran, Perunninakulath S.,Tilve, Santosh G.

experimental part, p. 6488 - 6490 (2011/02/23)

A cascade Wittig reaction-double Claisen and Cope rearrangements has been employed for a one-pot synthesis of diprenylated coumarins gravelliferone, balsamiferone, and 6,8-diprenylumbelliferone from a common precursor 2,4-diprenyloxybenzaldehyde.

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