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53005-18-8

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53005-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53005-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,0 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53005-18:
(7*5)+(6*3)+(5*0)+(4*0)+(3*5)+(2*1)+(1*8)=78
78 % 10 = 8
So 53005-18-8 is a valid CAS Registry Number.

53005-18-8SDS

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 1,5-dimethoxypentan-3-one

1.2 Other means of identification

Product number -
Other names 1,5-dimethoxy-pentan-3-one

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:53005-18-8 SDS

53005-18-8Relevant articles and documents

Iron-catalyzed urea synthesis: Dehydrogenative coupling of methanol and amines

Lane, Elizabeth M.,Hazari, Nilay,Bernskoetter, Wesley H.

, p. 4003 - 4008 (2018/05/04)

Substituted ureas have numerous applications but their synthesis typically requires the use of highly toxic starting materials. Herein we describe the first base-metal catalyst for the selective synthesis of symmetric ureas via the dehydrogenative coupling of methanol with primary amines. Using a pincer supported iron catalyst, a range of ureas was generated with isolated yields of up to 80% (corresponding to a catalytic turnover of up to 160) and with H2 as the sole byproduct. Mechanistic studies indicate a stepwise pathway beginning with methanol dehydrogenation to give formaldehyde, which is trapped by amine to afford a formamide. The formamide is then dehydrogenated to produce a transient isocyanate, which reacts with another equivalent of amine to form a urea. These mechanistic insights enabled the development of an iron-catalyzed method for the synthesis of unsymmetric ureas from amides and amines.

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