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3,3-DiMethoxythietane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89280-54-6

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89280-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89280-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,8 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89280-54:
(7*8)+(6*9)+(5*2)+(4*8)+(3*0)+(2*5)+(1*4)=166
166 % 10 = 6
So 89280-54-6 is a valid CAS Registry Number.

89280-54-6SDS

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 Thietane, 3,3-dimethoxy-

1.2 Other means of identification

Product number -
Other names 3-Thietanone, dimethyl acetal

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:89280-54-6 SDS

89280-54-6Downstream Products

89280-54-6Relevant academic research and scientific papers

Diverse ring opening of thietanes and other cyclic sulfides: An electrophilic aryne activation approach

Zheng, Tianyu,Tan, Jiajing,Fan, Rong,Su, Shuaisong,Liu, Binbin,Tan, Chen,Xu, Kun

supporting information, p. 1303 - 1306 (2018/02/14)

Organosulfides are a common class of structure units in bioactive molecules and functional materials motivating continuous developments of efficient synthetic methods. Herein, we report an electrophilic aryne-activated ring opening protocol of one or two

Synthesis and structural analysis of a new class of azaspiro[3.3]heptanes as building blocks for medicinal chemistry

Burkhard, Johannes A.,Guerot, Carine,Knust, Henner,Rogers-Evans, Mark,Carreira, Erick M.

supporting information; experimental part, p. 1944 - 1947 (2010/07/04)

Figure presented Straightforward access toward previously unreported substituted, heterocyclic spiro[3.3]heptanes is disclosed. These spirocyclic systems may be considered as alternatives to 1,3-heteroatom-substituted cyclohexanes, which are otherwise insufficiently stable to allow their use in drug discovery. Conformational details are discussed on the basis of X-ray crystallographic structures.

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