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66982-46-5

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66982-46-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66982-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,8 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66982-46:
(7*6)+(6*6)+(5*9)+(4*8)+(3*2)+(2*4)+(1*6)=175
175 % 10 = 5
So 66982-46-5 is a valid CAS Registry Number.

66982-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-3-hydroxythietane

1.2 Other means of identification

Product number -
Other names 3-PHENYLTHIETAN-3-OL

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:66982-46-5 SDS

66982-46-5Relevant articles and documents

Synthesis of 1-Pyrroline by Denitrogenative Ring Expansion of Cyclobutyl Azides under Thermal Conditions

Ban, Kazuho,Miki, Yuya,Sajiki, Hironao,Sawama, Yoshinari,Tomita, Naohito

supporting information, p. 3481 - 3484 (2021/06/17)

We herein report an efficient and systematic synthesis of 1-pyrrolines from cyclobutyl azides under thermal and neutral conditions. The reaction proceeded without any additional reagents, and nitrogen was generated as the sole by-product. Furthermore, the generated 1-pyrrolines could be continuously transformed into pyrroles, N-Boc-amines, and oxaziridines in an one-pot manner. (Figure presented.).

Parallel Approaches for the Functionalization of Thietes: α-Metalation versus C-H Activation

Eisold, Michael,Müller-Deku, Adrian,Reiners, Felix,Didier, Dorian

supporting information, p. 4654 - 4658 (2018/08/07)

For the first time, an approach to 3,4-disubstituted thietes was developed through two complementary paths. While the first one relies on α-metalation, the second is based on direct C-H functionalization. A new library of sophisticated sulfur-containing four-membered rings is described, paving the way to new bioactive analogues and small heterocycle incorporation.

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