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60166-72-5

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60166-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60166-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,6 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60166-72:
(7*6)+(6*0)+(5*1)+(4*6)+(3*6)+(2*7)+(1*2)=105
105 % 10 = 5
So 60166-72-5 is a valid CAS Registry Number.

60166-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbuta-1,2-dienylcyclopropane

1.2 Other means of identification

Product number -
Other names 1-cyclopropyl-3-methyl-1,2-butadiene

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:60166-72-5 SDS

60166-72-5Downstream Products

60166-72-5Relevant articles and documents

Polylithiumorganic compounds - 23. 1: 3,4-dilithio-1,2-butadienes by addition of lithium metal to 1,4-unsymmetrically substituted butatrienes

Maercker, Adalbert,Wunderlich, Hans,Girreser, Ulrich

, p. 6149 - 6172 (2007/10/03)

The synthesis of the highly reactive 1,4-unsymmetrically substituted butatrienes 12a-c is described. When employing a strict synthetic protocol, these alkatrienes react with lithium metal to 3,4-dilithio-1,2-butadienes 20a-c as stable intermediates. The structure of 20 is supported by IR and NMR spectroscopic evidence. The same dianionic intermediate can be prepared in one case by double deprotonation of the 1,2-butadiene 19. Upon derivatization, either 3,4-disubstituted 1,2-butadienes 24, 2,3-disubstituted 1,3-butadienes 25, or 1,4-disubstituted 2-butynes 26 are formed, depending on the nature of the electrophile employed. Copyright

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