Home Cart Sign in  
Chemical Structure| 198545-76-5 Chemical Structure| 198545-76-5
Chemical Structure| 198545-76-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Fmoc-D-Phe(4-Br)-OH

CAS No. :198545-76-5
Formula : C24H20BrNO4
M.W : 466.32
SMILES Code : O=C(O)[C@@H](CC1=CC=C(Br)C=C1)NC(OCC2C3=CC=CC=C3C4=CC=CC=C24)=O
MDL No. :MFCD00273459
InChI Key :TVBAVBWXRDHONF-JOCHJYFZSA-N
Pubchem ID :7020431

Safety of Fmoc-D-Phe(4-Br)-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Fmoc-D-Phe(4-Br)-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 198545-76-5 ]

[ 198545-76-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 198545-76-5 ]
  • [ 214360-60-8 ]
  • (R)-2-amino-(9-fluorenylmethoxycarbonyl)amino-3-(4'-acetamido-[1,1'-biphenyl]-4-yl)propanoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% With sodium carbonate; palladium dichloride; In tetrahydrofuran; ethylene glycol; at 66℃; for 3h;Inert atmosphere; Compound 4(64 mg, 0.25 mmol) was dissolved in a mixture of tetrahydrofuran andethylene glycol (10:1, 15 mL) at rt. N-(9-Fluorenylmethoxycarbonyl)-4-bromo-D-phenylalanine (5, 96 mg, 0.21 mmol) was added and the mixturewas kept stirring. PdCl2 (10 mol %, 4 mg) was added and nitrogen was bubbledthrough the reaction mixture for 15 min. Na2CO3 (66 g, 0.62 mmol) was thenadded into the reaction mixture whereupon the flask was filled with nitrogenand heated at 66 C for 3 h. When the TLC showed completion of the reactionwater (20 mL) was added into the reaction mixture which was then extractedwith ethyl acetate (3 30 mL). The combined organic layers were washed withbrine-water (1:1, 2 25 mL), dried over Na2SO4 and concentrated to drynessunder reduced pressure. The crude product was purified by columnchromatography (2-3% MeOH in DCM containing 0.1% AcOH) to affordcompound 6 (87 mg, 81%).
 

Historical Records

Technical Information

Categories