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1223573-30-5

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1223573-30-5 Usage

General Description

Ethyl 2-(thietan-3-ylidene)acetate is a chemical compound with the molecular formula C7H10O2S. It is also known as ethyl 3-thietanecarboxylate and is classified as an ester. Ethyl 2-(thietan-3-ylidene)acetate is commonly used in the fragrance and flavor industry, and it is known for its fruity and sulfurous aroma. It can be found in various fruits and vegetables, and it is often added to perfumes and food products to impart a tropical or citrusy scent. Ethyl 2-(thietan-3-ylidene)acetate is considered safe for use in these applications and is widely used in the production of consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 1223573-30-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,5,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1223573-30:
(9*1)+(8*2)+(7*2)+(6*3)+(5*5)+(4*7)+(3*3)+(2*3)+(1*0)=125
125 % 10 = 5
So 1223573-30-5 is a valid CAS Registry Number.

1223573-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name thietan-3-ylidene-acetic acid ethyl ester

1.2 Other means of identification

Product number -
Other names Ethyl 2-(thietan-3-ylidene)acetate

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:1223573-30-5 SDS

1223573-30-5Relevant articles and documents

Synthesis of 6-Azaspiro[4.3]alkanes: Innovative Scaffolds for Drug Discovery

Chalyk, Bohdan A.,Isakov, Andrei A.,Butko, Maryna V.,Hrebeniuk, Kateryna V.,Savych, Olena V.,Kucher, Olexandr V.,Gavrilenko, Konstantin S.,Druzhenko, Tetiana V.,Yarmolchuk, Vladimir S.,Zozulya, Sergey,Mykhailiuk, Pavel K.

, p. 4530 - 4542 (2017/08/30)

New scaffolds for drug discovery, 6-azaspiro[4.3]alkanes, have been synthesized in two steps from four-membered-ring ketones: cyclobutanone, thienone, N-Boc-azetidinone (Boc = tert-butoxycarbonyl), etc. The key transformation was the reaction between electron-deficient exocyclic alkenes and an in-situ generated N-benzylazomethine ylide.

AZA-OXO-INDOLES FOR THE TREATMENT AND PROPHYLAXIS OF RESPIRATORY SYNCYTIAL VIRUS INFECTION

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Page/Page column 119, (2014/12/12)

The invention provides compounds having the general formula: wherein R1, R2, R3, R4, R5, R6, W1, W2, W3, A and X are as described herein, compositions including the compounds and methods of using the compounds.

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