
37440-01-0
- Product Name:(R)-N-Acetyl-2-naphthylalanine
- Molecular Formula:C15H15NO3
- Purity:99%
- Molecular Weight:257.289
Product Details;
CAS#: 37440-01-0
Molecular Formula: C15H15NO3
Appearance: off-white to light yellow-beige granular powder
Trustworthy Factory Supply Reliable Quality 37440-01-0 with Cheapest Price
- Molecular Formula:C15H15NO3
- Molecular Weight:257.289
- Appearance/Colour:off-white to light yellow-beige granular powder
- Vapor Pressure:1.21E-12mmHg at 25°C
- Refractive Index:1.5200 (estimate)
- Boiling Point:543.438 °C at 760 mmHg
- PKA:3.59±0.30(Predicted)
- Flash Point:282.461 °C
- PSA:66.40000
- Density:1.244 g/cm3
- LogP:2.36250
(R)-N-Acetyl-2-naphthylalanine(Cas 37440-01-0) Usage
InChI:InChI=1/C15H15NO3/c1-10(17)16-14(15(18)19)9-11-6-7-12-4-2-3-5-13(12)8-11/h2-8,14H,9H2,1H3,(H,16,17)(H,18,19)/p-1/t14-/m1/s1
37440-01-0 Relevant articles
The Enantioselective Dakin-West Reaction
Wende, Raffael C.,Seitz, Alexander,Niedek, Dominik,Schuler, S?ren M. M.,Hofmann, Christine,Becker, Jonathan,Schreiner, Peter R.
, p. 2719 - 2723 (2016/02/27)
Here we report the development of the fi...
Preparation of cross-linked enzyme aggregates of l-aminoacylase via co-aggregation with polyethyleneimine
Vaidya, Bhalchandra K.,Kuwar, Suyog S.,Golegaonkar, Sandeep B.,Nene, Sanjay N.
experimental part, p. 184 - 191 (2012/03/22)
l-Aminoacylase from Aspergillus melleus ...
Convenient method for reduction of C-N double bonds in oximes, imines, and hydrazones using sodium Borohydride-Raney ni system
Yang, Yihua,Liu, Shouxin,Li, Junzhang,Tian, Xia,Zhen, Xiaoli,Han, Jianrong
experimental part, p. 2540 - 2554 (2012/07/27)
(Chemical Equation Presented) A practica...
CHIRAL PHOSPHORUS COMPOUNDS
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Page/Page column 37-39, (2008/12/04)
The present invention provides P-chiral ...
37440-01-0 Process route
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- 37439-99-9,37440-01-0,58438-02-1
(RS)-N-acetyl-2-naphthylalanine

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- 6960-34-5,14108-60-2,58438-03-2,76985-09-6,106107-92-0
L-3-(2-naphthyl)alanine

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- 76985-09-6,106107-92-0
(R)-2-naphthylalanine

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- 37440-01-0
(R)-2-acetamido-3-(naphthalen-2-yl)propanoic acid
Conditions | Yield |
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With cobalt(II) chloride; at 30 ℃; pH=8; optical yield given as %ee; enantioselective reaction; aq. phosphate buffer; Resolution of racemate; Enzymatic reaction;
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(Z)-2-acetamido-3-(naphthalen-2-yl)acrylic acid

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- 37440-01-0
(R)-2-acetamido-3-(naphthalen-2-yl)propanoic acid
Conditions | Yield |
---|---|
With <(1R)-phenylethyl-FERRIPHOS>; hydrogen; rhodium(I)-bis(1,5-cyclooctadiene) tetrafluoroborate; In methanol; under 750.06 Torr;
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With hydrogen;
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With [rhodium(I)(norborna-2,5-diene)2]SbF6; hydrogen; (1S,1S',2R,2R')-1,1'-di-tert-butyl-(2,2’)-diphospholane; In methanol; at 20 ℃; for 12h; under 1034.3 Torr;
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37440-01-0 Upstream products
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1353886-59-5
ethyl 2-(hydroxyimino)-3-(naphthalen-3-yl)propanoate
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14108-60-2
2-amino-3-(2-naphthyl)propanoic acid
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108-24-7
acetic anhydride
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37447-33-9
acetylamino-[2]naphthylmethyl-malonic acid diethyl ester
37440-01-0 Downstream products
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6960-34-5
L-3-(2-naphthyl)alanine
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76985-09-6
(R)-2-naphthylalanine
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292141-31-2
Ac-D-Nal2-D-Cpa-D-Pal-Gly-Arg-Pro-D-Ala-NH2
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292141-25-4
Ac-D-Nal2-D-Cpa-D-Pal-D-Ala-Lys-Pro-D-Ala-NH2
Relevant Products
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Fmoc-L-Ala-OH·H2O
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FMOC-THR(TBU)-OL
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Fmoc-3-(2-Naphthyl)-D-alanine
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