Cas 1103424-24-3,(E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate

1103424-24-3

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Basic information

Product Name: (E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate
Synonyms: (E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate
CAS NO:1103424-24-3
Molecular Formula:
Molecular Weight: 341.202
EINECS: N/A
Product Categories: N/A

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: (E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate(1103424-24-3)
EPA Substance Registry System: (E)-dimethyl 2-[1-(1-bromomethylidene)-3-phenylpropyl]malonate(1103424-24-3)

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: 1103424-24-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1103424-24-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,3,4,2 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1103424-24:
(9*1)+(8*1)+(7*0)+(6*3)+(5*4)+(4*2)+(3*4)+(2*2)+(1*4)=83
83 % 10 = 3
So 1103424-24-3 is a valid CAS Registry Number.

1103424-24-3Upstream product

849371-52-4 dimethyl 2-(2-phenylethyl)cycloprop-2-ene-1,1-dicarboxylate

1103424-24-3Downstream Products

1103424-24-3Relevant academic research and scientific papers

Stereoselective formation of alkenyl halides via magnesium halide promoted ring opening of bis-activated cyclopropenes

Wang, Yi,Lam, Hon Wai

supporting information; experimental part, p. 1353 - 1355 (2009/07/04)

In the presence of stoichiometric magnesium halides, a range of bis-activated cyclopropenes undergo highly stereoselective ring-opening reactions to produce multisubstituted alkenyl halides. More highly functionalized compounds may be obtained by trapping

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