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6142-38-7

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6142-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6142-38-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6142-38:
(6*6)+(5*1)+(4*4)+(3*2)+(2*3)+(1*8)=77
77 % 10 = 7
So 6142-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H12N2O7/c1-8-2-5-12(13(6-8)18(24)25)17-14(19)11-7-9(15(20)21)3-4-10(11)16(22)23/h2-7H,1H3,(H,17,19)(H,20,21)(H,22,23)

6142-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxypropanal

1.2 Other means of identification

Product number -
Other names 2-Methoxy-propionaldehyd

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:6142-38-7 SDS

6142-38-7Downstream Products

6142-38-7Relevant articles and documents

FACTORS AFFECTING REGIOSLECTIVITY IN THE RHODIUM-CATALYSED HYDROFORMYLATION OF VINYL ETHERS

Lazzaroni, Raffaelo,Bertozzi, Sergio,Pocai, Paolo,Troiani, Francesco,Salvadori, Piero

, p. 371 - 376 (2007/10/02)

The rhodium catalysed hydroformylation of vinyl ethers ROCH=CH2, where R is an alkyl, a benzyl or a phenyl group, has been investigated over the 20-100 deg C temperature range in the presence of Rh4(CO)12 or 2/PPh3 (1/6) as catalytic precursors.A mixture of 2-alkoxy-(or phenoxy)propanal (the α-isomer) and 3-alkoxy-(or phenoxy)propanal (the β-isomer) is obatined in good yield.The isomeric composition of the aldehydes depends on the structure of the substrate, on the catalytic precursor employed, and on the reaction temperature.The α-isomer predomines in all the cases, its predominance being greater (i) at low temperatures, (ii)in the presence of Rh4(CO)12 as catalyst precursor, and (iii) when a phenyl group is present in the β or γ position with respect to the double bond in the substrate.Electronic factors arising from the presence in the substrate of the oxygen atom and a phenyl group are more impotrant than the steric hindrance of tghe R group in detrmining the regioselectivity of the reaction.

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