Cas 74544-86-8,(2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine

74544-86-8

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Basic information

Product Name: (2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine
Synonyms: (2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine
CAS NO:74544-86-8
Molecular Formula:
Molecular Weight: 373.09
EINECS: N/A
Product Categories: N/A
Mol File: 74544-86-8.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine(CAS DataBase Reference)
NIST Chemistry Reference: (2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine(74544-86-8)
EPA Substance Registry System: (2,6-Dibromo-phenyl)-(4,5-dihydro-1H-imidazol-2-yl)-(2-methyl-allyl)-amine(74544-86-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 74544-86-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74544-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,4 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74544-86:
(7*7)+(6*4)+(5*5)+(4*4)+(3*4)+(2*8)+(1*6)=148
148 % 10 = 8
So 74544-86-8 is a valid CAS Registry Number.

74544-86-8Upstream product

4205-93-0 2-<(2,6-dibromophenyl)imino>imidazolidine

74544-86-8Downstream Products

74544-86-8Relevant articles and documents

Chemistry, Pharmacology, and Structure-Activity Relationships with a New Type of Imidazolines Exerting a Specific Bradycardic Action at a Cardiac Site

Staehle, Helmut,Daniel, Helmut,Kobinger, Walter,Lillie, Christian,Pichler, Ludwig

, p. 1217 - 1222 (2007/10/02)

The reaction of alkyl halides with 2-(arylimino)imidazolidines (I) leads to imidazoline derivatives II, in which the side chain is situated at the bridge nitrogen atom between the phenyl group and the imidazoline ring.The new imidazolines (II) exert a spe

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