179251-28-6 Usage
Explanation
The compound's name is derived from its structure, which includes a bromine atom at the 1st position, a cyclopropylmethyl group at the 4th position, and a benzene ring.
Explanation
This is an alternative name for the compound, which is used interchangeably.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and bromine (Br) atoms in the compound, which are 10, 11, and 1, respectively.
Explanation
The compound is a liquid at room temperature and is colorless in appearance.
Explanation
1-Bromo-4-(cyclopropylmethyl)-benzene is mainly used as a starting material for the synthesis of various chemicals.
Explanation
The compound is used as a building block in the synthesis of pharmaceuticals, agrochemicals, and dyes due to its versatile chemical structure.
Explanation
It is also utilized in the production of polymers and other organic compounds, showcasing its versatility in organic synthesis.
Explanation
The compound has potential applications in the field of medicinal chemistry, possibly due to its unique structure and reactivity.
Explanation
Due to its toxic nature, proper safety measures should be taken when handling 1-Bromo-4-(cyclopropylmethyl)-benzene to prevent ingestion, inhalation, or skin contact.
Synonyms
1-bromo-4-(cyclopropylmethyl)benzene
Physical state
Colorless liquid
Primary use
Intermediate in chemical production
Applications
Pharmaceutical, agrochemical, and dye production
Additional use
Polymer and organic compound manufacturing
Potential applications
Medicinal chemistry
Safety precautions
Toxic and harmful if swallowed, inhaled, or absorbed through the skin
Check Digit Verification of cas no
The CAS Registry Mumber 179251-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,2,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 179251-28:
(8*1)+(7*7)+(6*9)+(5*2)+(4*5)+(3*1)+(2*2)+(1*8)=156
156 % 10 = 6
So 179251-28-6 is a valid CAS Registry Number.
179251-28-6Relevant articles and documents
Facile preparation of cyclopropanes from 2-iodoethyl-substituted olefins and 1,3-dihalopropanes with zinc powder
Sakuma, Daisuke,Togo, Hideo
, p. 10138 - 10145 (2005)
Two efficient, simple, cheap, and environmentally benign preparations of cyclopropanes were achieved. One is the formation via 3-exo-trig manner from various electron-deficient 2-iodoethyl-substituted olefins with zinc powder in a mixture of t-butyl alcoh
NOVEL DICARBOXYLIC ACID DERIVATIVES AS S1P1 RECEPTOR AGONISTS
-
, (2009/01/24)
The present invention relates to new compounds of formula (I) possessing agonistic activity at sphingosine-1 -phosphate (S1 P) receptors, their process of preparation and their use as immunosuppressive agents. The invention is also directed to pharmaceutical compositions containing these compounds and use of these compounds for treatment/prevention of immune mediated diseases and conditions or inflammatory diseases and conditions.
PHENYL SULFONAMIDE ENDOTHELIN ANTAGONISTS
-
, (2008/06/13)
Compounds of the formula STR1 inhibit the activity of endothelin. The symbols are defined as follows: R 1, R 2 and R. sup.3 are each independently(a) hydrogen, except that R. sup.1 is other than hydrogen;(b) alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, cycloalkylalkyl, cycloalkenyl, cycloalkenylalkyl, aryl, aryloxy, aralkyl or aralkoxy, any of which may be substituted with Z 1, Z 2 and Z. sup.3 ;(c) halo;(d) hydroxyl;(e) cyano; (f) nitro; (g)--C(O)H or--C(O)R 6 ;(h)--CO 2 H or--CO 2 R 6 ; (i)--SH,--S(O) n R 6,--S(O) m--OH,--S(O) m--OR 6,--O--S(O) m--R 6,--O--S(O) m OH or--O--S(O) m--OR. sup.6 ;(j)--Z. sup.4--NR 7 R 8 ; or (k)--Z 4--N(R 11--Z 5--NR 9 R 10 ; and the remaining symbols are as defined in the specification.
