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16851-30-2

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16851-30-2 Usage

General Description

(3,3-Diethoxypropyl)dimethylamine is a chemical compound with the molecular formula C9H21NO2. It is a tertiary amine, which means it has three alkyl groups attached to the nitrogen atom. The compound is commonly used as a catalyst or intermediate in organic synthesis and chemical reactions. It is a colorless liquid with a slightly fruity odor and is soluble in organic solvents. (3,3-Diethoxypropyl)dimethylamine is also known for its ability to act as a corrosion inhibitor in some applications. It is important to handle this chemical with care and follow safety guidelines when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 16851-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,5 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16851-30:
(7*1)+(6*6)+(5*8)+(4*5)+(3*1)+(2*3)+(1*0)=112
112 % 10 = 2
So 16851-30-2 is a valid CAS Registry Number.

16851-30-2SDS

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 3,3-diethoxy-N,N-dimethylpropan-1-amine

1.2 Other means of identification

Product number -
Other names N-Diethylpropylacetal-N,N'-dimethylamin

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:16851-30-2 SDS

16851-30-2Relevant articles and documents

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Pailer,M. et al.

, p. 891 - 901 (1968)

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Selective Monomethylation of Amines with Methanol as the C1 Source

Choi, Geunho,Hong, Soon Hyeok

supporting information, p. 6166 - 6170 (2018/04/30)

The N-monomethyl functionality is a common motif in a variety of synthetic and natural compounds. However, facile access to such compounds remains a fundamental challenge in organic synthesis owing to selectivity issues caused by overmethylation. To address this issue, we have developed a method for the selective, catalytic monomethylation of various structurally and functionally diverse amines, including typically problematic primary aliphatic amines, using methanol as the methylating agent, which is a sustainable chemical feedstock. Kinetic control of the aliphatic amine monomethylation was achieved by using a readily available ruthenium catalyst at an adequate temperature under hydrogen pressure. Various substrates including bio-related molecules and pharmaceuticals were selectively monomethylated, demonstrating the general utility of the developed method.

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