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trans,trans-Farnesyl bromide / 1 G

Purity: 95 %
Synonym: trans,trans-1-Bromo-3,7,11-trimethyl-2,6,10-dodecatriene; Farnesyl bromide; e,e-farnesyl bromide; 2E,6E-Farnesyl Bromide; (2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-triene
Molecular Formula: (CH3)2C'=CH[CH2CH2C(CH3)'=CH]2CH2Br
Molecular Weight: 285.26
SKU: MND-51038
CAS Number: 28290-41-7
MDL number: MFCD00054465
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 1 G  
74.20 EUR



Safety Information


Hazard Statements

H315
H335
H318

Precautionary Statements

P280
P264
P501
P305 + P351 + P338
P261
P271
P405
P302 + P352
P362 + P364
P403 + P233
P304 + P340
P321
P264 + P265
P319
P332 + P317
P317

Pictograms



Properties

Signal WordDanger
Flash Point (C)113 °C - closed cup
Flash Point (F)235.4 °F - closed cup
Density1.052 g/mL at 25 °C (lit.)
Boiling Point100-110 °C/15 mmHg (lit.)

 Product Description

trans,trans-Farnesyl bromide is an organic compound featuring a brominated farnesyl group. It is used in organic synthesis and chemical research due to its reactivity and structural properties.

 

Application:

trans,trans-Farnesyl bromide is used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and other complex organic molecules.

 

 

Articles:

- Toxicity and Sublethal Effect of Farnesyl Acetate on Diamondback Moth, Plutella xylostella (L.) (Lepidoptera: Plutellidae)

Publication Date: 27 January 2021

Norazila Yusoff, Idris Abd Ghani, Nurul Wahida Othman, Wan Mohd Aizat and Maizom Hassan

https://doi.org/10.3390/insects12020109

 

- Synthesis and antimicrobial activity of geranyloxy- and farnesyloxy-acetophenone derivatives against oral pathogens

Publication Date: Available online 11 June 2012

Laetitia Bonifait, Annie Marquis, Salvatore Genovese, Francesco Epifano, Daniel Grenier

https://doi.org/10.1016/j.fitote.2012.06.003

 

- Synthesis and biological evaluation of farnesylthiosalicylamides as potential anti-tumor agents

Publication Date:

Yong Ling, Zhiqiang Wang, Hongyan Zhu, Xuemin Wang, Wei Zhang, Xinyang Wang, Li Chen, Zhangjian Huang, Yihua Zhang

https://doi.org/10.1016/j.bmc.2013.11.013