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19070-16-7

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19070-16-7 Usage

General Description

Chloro[3-(dimethylamino)propyl]magnesium is a chemical compound with an interesting arrangement of atoms and functional groups. It contains chlorine, magnesium, and the functional group -N(CH3)2, also known as a dimethylamino group. This functional group is attached to a three-carbon propyl group. As an organomagnesium compound, it may behave as a strong base and nucleophile, potentially making it useful in certain chemical reactions. Specific properties such as its physical state, color, odor, melting point, boiling point, density, solubility, and stability under various conditions may vary depending on its precise formulation and any stabilizing agents that may be added. Its applications and safety measures would depend on these characteristics and the specific ways in which the compound is used.

Check Digit Verification of cas no

The CAS Registry Mumber 19070-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19070-16:
(7*1)+(6*9)+(5*0)+(4*7)+(3*0)+(2*1)+(1*6)=97
97 % 10 = 7
So 19070-16-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N.ClH.Mg/c1-4-5-6(2)3;;/h1,4-5H2,2-3H3;1H;/q;;+1/p-1/rC5H12ClMgN/c1-8(2)5-3-4-7-6/h3-5H2,1-2H3

19070-16-7SDS

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 magnesium,N,N-dimethylpropan-1-amine,chloride

1.2 Other means of identification

Product number -
Other names CHLORO[3-(DIMETHYLAMINO)PROPYL]MAGNESIUM

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:19070-16-7 SDS

19070-16-7Relevant articles and documents

Synthesis of new heteroleptic strontium complexes

George, Sheby Mary,Kim, Hyo-Suk,Park, Bo Keun,Kim, Chang Gyoun,Chung, Taek-Mo,Lah, Myoung Soo

, p. 14461 - 14469 (2014)

A series of heteroleptic strontium complexes (1-9) using a combination of different aminoalkoxides and 2,2,6,6-tetramethyl-3,5-heptanedionate (tmhd) were prepared to examine the effect of the bulkiness and coordination ability of the aminoalkoxide ligand in these complexes as well as potential strontium precursors. All complexes were characterized by FT-IR, FT-NMR, elemental analyses, and thermo-gravimetric (TG) analyses. The crystal structure analyses of 1, 2, 4, and 5 demonstrate their stability in the dimer form and the unwillingness of the strontium atom to form more than six coordination bonds in these complexes. The complex 5 shows an unusual picture: the existence of one hexa-coordinated and one penta-coordinated strontium atom side by side in its dimer structure. The introduction of ether groups as coordination sites in complexes 6-9 led to a decrease in steric hindrance which resulted in the formation of the complex 7 as a tetramer. The complex 7 shows a unique Sr4O4cubane core where oxygen atoms undergo μ3-bridging between strontium atoms. The TG analyses show that the complexes exhibit a step-wise decomposition character, with the major mass losses in the region 150-400 °C.

NOVEL PHTHALOCYANINE DERIVATIVES FOR THERAPEUTIC USE

-

Page/Page column 10; 11, (2013/03/26)

There are described phthalocyanine derivates, the pharmaceutical compositions and the medical devices that contain them, possibly in combination with chelating agents, such as EDTA, useful for treating, by means of photodynamic therapy, diseases character

Preparation of Escitalopram, Its Salts and Intermediates

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Page/Page column 6, (2011/05/03)

The present patent application relates to an improved process for the preparation of escitalopram, its salts and intermediates. It also relates to a novel crystalline form S of citalopram diol intermediate, process for preparation and its use in the preparation of citalopram, escitalopram and their salts.

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