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52829-88-6

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52829-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52829-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,2 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52829-88:
(7*5)+(6*2)+(5*8)+(4*2)+(3*9)+(2*8)+(1*8)=146
146 % 10 = 6
So 52829-88-6 is a valid CAS Registry Number.

52829-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dimethoxy-1-cyclopropylethane

1.2 Other means of identification

Product number -
Other names (1,1-dimethoxy-ethyl)-cyclopropane

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:52829-88-6 SDS

52829-88-6Relevant articles and documents

Ag(i)-Catalyzed rapid access to 2-amino-4-methylenethiazolines with potential applications in bioconjugation chemistry

Xiang, Lingling,Wu, Haiting,Liang, Yunshi,Deng, Huiying,He, Yiting,Xu, Qin,Zhang, Jing

, p. 4060 - 4066 (2021)

An Ag(i)-catalyzed tandem addition-cyclization of isothiocyanate and propargylamine was successfully applied to the synthesis of 2-amino-4-methylenethiazolines. This route features an unprecedented fast reaction rate with full conversion reached within 10

SYNTHESIS AND ELABORATION OF HETEROCYCLES VIA IODOCYCLISATION OF UNSATURATED THIOUREAS

Creeke, Paul I.,Mellor, John M.

, p. 4435 - 4438 (2007/10/02)

Iodocyclisation of N-allyl or S-allyl thioureas leads efficiently to dihydrothiazoles, and dihydroimidazoles and homologous thioureas afford dihydrothiazines.The products are readily elaborated to give unusual heterocyclic systems.

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