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3,4-(Methylenedioxy)phenylmagnesium bromide / 100ml

Purity: 0.50 M in 2'=MeTHF
Molecular Formula: C7H5BrMgO2
Molecular Weight: 225.32
SKU: MND-127655
CAS Number: 17680-04-5
MDL number: MFCD01863705
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 100ml  
163.80 EUR



Safety Information


Hazard Statements

H225
H302
H314
H313

Precautionary Statements

P210
P280
P270
P331
P271
P240
P242
P243
P264b
P304 + P340
P305 + P351 + P338
P330
P362 + P364
P403 + P233
P501c
P303 + P361 + P353

Pictograms

 Product Description

3,4-(METHYLENEDIOXY)PHENYLMAGNESIUM BROMIDE is a chemical compound commonly employed in organic synthesis as a Grignard reagent. It serves as a crucial precursor in the formation of complex organic molecules.

 

Application:

Utilized as a Grignard reagent, 3,4-(METHYLENEDIOXY)PHENYLMAGNESIUM BROMIDE plays a pivotal role in organic synthesis, facilitating the introduction of the 3,4-(methylenedioxy)phenyl group into various organic compounds.

 

 

 Articles:

-14C-labeling of a novel atypical β-adrenoceptor agonist, SM-11044

Publication Date: March 1996

Motohiro Kurosawa, Hiroshi Kanamaru, Kazuhiko Nishioka

-https://doi.org/10.1002/(SICI)1099-1344(199603)38:3<285::AID-JLCR836>3.0.CO;2-P

 

-Total Synthesis and Stereochemical Confirmation of Manassantin A, B, and B1

Publication Date: October 24, 2006

Stephen Hanessian, Gone Jayapal Reddy, and Navjot Chahal

-https://doi.org/10.1021/ol0621710

 

-Structure-activity relationships of talaumidin derivatives: Their neurite-outgrowth promotion in vitro and optic nerve regeneration in vivo

Publication Date: 25 March 2018

Kenichi Harada, Katsuyoshi Zaha, Rina Bando, Ryo Irimaziri, Miwa Kubo, Yoshiki Koriyama, Yoshiyasu Fukuyama

-https://doi.org/10.1016/j.ejmech.2018.02.014