18977-45-2 Usage
General Description
"(Cyclopropylmethyl)methylamine" is a chemical compound with a molecular formula of C6H11N. It is a volatile, flammable, and potentially explosive liquid with a strong odor. (cyclopropylmethyl)methylamine(SALTDATA: FREE) is primarily used in the production of various pharmaceuticals and pesticides. It is also used as a building block in the synthesis of other chemical compounds. The safety data for this compound indicates that it should be handled with care due to its flammable and potentially explosive nature. It also presents risks for inhalation, skin contact, and ingestion, so proper protective measures should be taken when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 18977-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,7 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18977-45:
(7*1)+(6*8)+(5*9)+(4*7)+(3*7)+(2*4)+(1*5)=162
162 % 10 = 2
So 18977-45-2 is a valid CAS Registry Number.
18977-45-2Relevant articles and documents
Enamine quaternary compounds, methods of making and their use as muscle relaxants
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, (2008/06/13)
Disclosed are novel enamine quaternary compounds of the formula STR1 wherein m=1, 2 or 3 and n=1, 2 or 3 with the proviso that m+n=3, 4 or 5; R1 and R2 are independently lower alkyl or hydrogen, and R3 and R4 are independently selected from the group consisting of lower alkyl, lower cycloalkyl lower alkyl, lower alkenyl, phenyl lower alkyl, thienyl lower alkyl, furyl lower alkyl, lower alkoxy lower alkyl, halogenated lower alkyl, lower alkyloyloxo or lower alkyloyloxy lower alkyl or wherein NR3 R4 together comprise a heterocycle ring; and wherein X- represents a pharmaceutically acceptable anion. Pharmaceutical compositions containing the same when administered to warm-blooded animals exhibit a muscle relaxant effect characterized by excellent onset and recovery times. Also disclosed are methods of making the enamine quaternary compounds.
