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FMOC-D-Valine

FMOC-D-Valine structure

FMOC-D-Valine 

structure
  • CAS No:

    84624-17-9

  • Formula:

    C20H21NO4

  • Chemical Name:

    FMOC-D-Valine

  • Synonyms:

    (R)-2-((((9H-fluoren-9-yl)Methoxy)carbonyl)aMino)-3-Methylbutanoic acid;Fmoc-D-Val-OH >=98.0% (HPLC);Fmoc-D-valine≥ 99% (HPLC);N-FMOC-D-VALINE;N-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]-D-VALINE;N-9-FLUORENYLMETHYLOXYCARBONYL-D-VALINE;N-(9-FLUORENYLMETHOXYCARBONYL)-D-VALINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-VALINE

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

white to light yellow crystal powde

FMOC-D-Valine Basic Attributes

339.39

339.147064

1533716-785-6

2924299090

Characteristics

75.6

4

White to off-white crystalline powder

1.2±0.1 g/cm3

143-144 °C(lit.)

287.5±25.4 °C

1.590

Solubility in methanol (almost transparency). Slightly soluble in water.

2-8°C

17 º (c=1, DMF)

Safety Information

NONH for all modes of transport

3

22-24/25

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

FMOC-D-Valine Use and Manufacturing

Take 500mL of the reaction bottle, Chiral amino acids R-3a (4.5 g, 38.9 mmol) were added to the reaction flask, respectively, Dioxane (40 mL) and10percent sodium carbonate (100 mL), The reaction flask was placed in an ice bath, Mechanical agitation, To the dropping funnel was added chloroform-9-fluorenylmethyl ester (10.0 g, 38.8 mmol)And dioxane (100 mL), Slowly drop into the reaction flask and gradually return to room temperature and stir overnight.After completion of the reaction, add water 100mL, extracted with 50mL ether three times, take the water phase into the ice bath to cool, add 1M dilute HCl to PH 1.The aqueous solution was extracted three times with 50 mL of ethyl acetate.The oil phase was combined and dried over magnesium sulfate, Filtration followed by drying to give intermediate R-4a (12.6 g, 96percent).

Computed Properties

Molecular Weight:339.4
XLogP3:4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:339.14705815
Monoisotopic Mass:339.14705815
Topological Polar Surface Area:75.6
Heavy Atom Count:25
Complexity:470
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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