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118486-95-6

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118486-95-6 Usage

General Description

5-Methyl-2-(tributylstannyl)furan is an organotin compound and a derivative of furan. It is a clear, colorless liquid at room temperature and is used as a reagent in organic synthesis. Its molecular structure consists of a furan ring with a methyl group and a tributylstannyl group attached at different positions. The tributylstannyl group makes it useful as a precursor in cross-coupling reactions for the synthesis of complex organic molecules. However, it is important to handle this compound with caution due to the toxic and hazardous nature of the tributylstannyl group.

Check Digit Verification of cas no

The CAS Registry Mumber 118486-95-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,4,8 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118486-95:
(8*1)+(7*1)+(6*8)+(5*4)+(4*8)+(3*6)+(2*9)+(1*5)=156
156 % 10 = 6
So 118486-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H5O.3C4H9.Sn/c1-5-3-2-4-6-5;3*1-3-4-2;/h2-3H,1H3;3*1,3-4H2,2H3;/rC17H32OSn/c1-5-8-13-19(14-9-6-2,15-10-7-3)17-12-11-16(4)18-17/h11-12H,5-10,13-15H2,1-4H3

118486-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methyl-2-(tributylstannyl)furan

1.2 Other means of identification

Product number -
Other names tributyl-(5-methylfuran-2-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:118486-95-6 SDS

118486-95-6Relevant articles and documents

Adenosine receptor antagonists

-

Paragraph 0117-0120, (2020/12/15)

The invention provides a compound shown as a formula (I) and a pharmaceutical composition thereof. The compounds of formula (I) of the present invention are useful as adenosine receptor inhibitors, especially A2A and/or A2B inhibitors, for example, the product can be used for prevention or treatment of diseases associated with A2A and/or A2B activity or expression.

P2X3 AND/OR P2X2/3 COMPOUNDS AND METHODS

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Paragraph 0231; 0232, (2015/07/07)

The present application provides novel compounds and methods for preparing and using these compounds. In one embodiment, the compounds are of the structure of formula (I), wherein R1-R4 are defined herein. In a further embodiment, these compounds are useful in method for regulating one or both of the P2X3 or P2X2/3 receptors. In another embodiment, these compounds are useful for treating pain in patients by administering one or more of the compounds to a patient.

Oxidative Substitution Reactions of Organostannyl Compounds with Lead Tetraacetate. A Convenient Route to 5-Alkylidene-2(5H)-furanones

Yamamoto, Makoto,Munakata, Hiroshi,Kishikawa, Keiki,Kohmoto, Shigeo,Yamada, Kazutoshi

, p. 2366 - 2370 (2007/10/02)

5-Substituted 2-tributylstannylfurans which were synthesized by the reaction of corresponding 5-substituted 2-lithiofurans with tribitylstannyl chloride, were treated with two equimolar amounts of lead tetraacetate at room temperature to give corresponding 5-substituted 5-acetoxy-2(5H)-furanones in good yields.The 5-acetoxy-2(5H)-furanone was heated at 80 deg C in acetic acid-acetic anhydride containing a catalytic amount of concentrated sulfuric acid to give 5-alkylidene-2(5H)-furanone in moderate yield.

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