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36215-07-3

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36215-07-3 Usage

Chemical Properties

Clear Colorless Liquid

Uses

1-Chloro-3-methoxypropane (cas# 36215-07-3) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 36215-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36215-07:
(7*3)+(6*6)+(5*2)+(4*1)+(3*5)+(2*0)+(1*7)=93
93 % 10 = 3
So 36215-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H9ClO/c1-6-4-2-3-5/h2-4H2,1H3

36215-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-3-methoxypropane

1.2 Other means of identification

Product number -
Other names 3-Chloropropyl methyl ether

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:36215-07-3 SDS

36215-07-3Relevant articles and documents

Synthesis, structural study, and in vitro trypanocidal and antitumour activities of tetrakis(3-methoxypropyl)tin and (3-methoxypropyl)tin chlorides

Lebl, Tomas,Smicka, Ales,Brus, Jiri,Bruhn, Clemens

, p. 143 - 148 (2003)

A set of four water-soluble (3-methoxypropyl)stannanes of general formula (CH3OCH2CH2CH2)x SnCl4-x, where x = 4 (1), x = 3 (2), x = 2 (3), and x = 1 (4), was prepared. For 3 and 4, which were isolated in the crystalline state, it was shown by X-ray diffraction that the tin atom is coordinated in distorted octahedral and trigonal-bipyramidal geometries, respectively (i.e., the oxygen atoms of the 3-methoxypropyl groups were coordinated to the central tin atom in both cases, forming chelates). For all compounds, structures in CDCl3 and [D6]DMSO solutions were proposed on the basis of their 13C and 119Sn NMR spectra. In CDCl3 solution, the degree of donor-acceptor bonding between the central tin atom and oxygen atom of the 3-methoxypropyl substituent was evaluated on the basis of 17O NMR chemical shifts and 3,6J(1H, 119Sn) long-range coupling constants. Compounds 2 and 3 exhibited promising in vitro antitumour and trypanocidal activities. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2003.

Asymmetric organocatalytic electrophilic phosphination

Nielsen, Martin,Jacobsen, Christian Borch,Jorgensen, Karl Anker

supporting information; experimental part, p. 3211 - 3214 (2011/05/17)

Meeting the challenge: The first asymmetric catalytic C*-P bond formation employing electrophilic phosphorus compounds has been developed using a catalytic amount of a dimeric cinchona alkaloid, and a subsequent one-pot process to deliver high stereoselectivities and good yields of α-quaternary α-phosphino β-amino acids (see scheme). 31P-NMR experiments suggest a novel reaction mechanism wherein a cinchona alkaloid nucleophilically activates the phosphorus electrophile. Copyright

INTERMEDIATE COMPOUND OF TECHNETIUM NITRIDE COMPLEX FOR RADIODIAGNOSTIC IMAGING

-

Page/Page column 6, (2010/07/04)

A bisphosphonoaminc compound represented by the following formula (I): wherein R1, R2, R3, R4 and R5 are independently an alkyl group having 1 to 6 carbon atoms, and n is an integer of 1 to 6, is extremely useful as an intermediate for preparing a technetium nitride complex for radiodiagnostic imaging.

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