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1-(Trimethylstannyl)naphthalene is an organotin compound characterized by the presence of a naphthalene ring and a trimethylstannyl group. This chemical is a colorless liquid with a molecular formula of C11H15Sn and a molecular weight of 243.95 g/mol. It is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through Stille coupling reactions. The compound is sensitive to air and moisture, and it is typically stored under an inert atmosphere. Due to its reactivity and potential toxicity, it is important to handle 1-(trimethylstannyl)naphthalene with care, using appropriate safety measures.

944-85-4

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944-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 944-85-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 944-85:
(5*9)+(4*4)+(3*4)+(2*8)+(1*5)=94
94 % 10 = 4
So 944-85-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H7.3CH3.Sn/c1-2-6-10-8-4-3-7-9(10)5-1;;;;/h1-7H;3*1H3;/rC13H16Sn/c1-14(2,3)13-10-6-8-11-7-4-5-9-12(11)13/h4-10H,1-3H3

944-85-4SDS

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 trimethyl(naphthalen-1-yl)stannane

1.2 Other means of identification

Product number -
Other names trimethyl-naphthalen-1-yl-stannane

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:944-85-4 SDS

944-85-4Relevant academic research and scientific papers

Polyarylcarbamoylaza- and -carbamoylalkanedioic acids

-

, (2008/06/13)

This invention relates to a class of novel dicarboxy amide derivatives of lipophilic amines which exhibit squalene synthase inhibition properties. More specifically the compounds are bis-aryl and/or heteroaryl alkyl or cycloalkylamino dicarboxy amides. Co

Reactions of Trialkylstannane Anions R3Sn- with Arylstannanes ArSnR'3

Mochida, Kunio

, p. 3299 - 3306 (2007/10/02)

The reactions of trialkylstannane anions R3Sn- with arylstannanes ArSnR'3 have been investigated; trialkylstannane anions with arylstannanes at 50 deg C gave substitution products ArSnR3 in good yields.Most of these substitution products are diverted to r

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