Nα-Boc-Nε-Azido-D-Lysine cyclohexylammonium salt
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Nα-Boc-Nε-Azido-D-Lysine cyclohexylammonium salt

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Category
BOC-Amino Acids
Catalog number
BAT-001327
CAS number
1620410-04-9
Molecular Formula
C17H33N5O4
Molecular Weight
371.50
IUPAC Name
(2R)-6-azido-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
Synonyms
(R)-6-Azido-2-(Boc-amino)hexanoic acid cyclohexylamine salt; Boc-6-azido-D-norleucine cyclohexylamine salt; Boc-D-Lys(N3)-OH CHA
Appearance
White crystalline powder
Purity
≥ 99% (HPLC)
Melting Point
121-126°C
Storage
Store at 2-8 °C
InChI
InChI=1S/C11H20N4O4/c1-11(2,3)19-10(18)14-8(9(16)17)6-4-5-7-13-15-12/h8H,4-7H2,1-3H3,(H,14,18)(H,16,17)/t8-/m1/s1
InChI Key
SKRPDWWWUARZIW-MRVPVSSYSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CCCCN=[N+]=[N-])C(=O)O
1. Bis(cyclohexylammonium) 2,2'-disulfanediyldibenzoate
Xinting Wei, Jing Li, Handong Yin Acta Crystallogr Sect E Struct Rep Online. 2011 Jan 12;67(Pt 2):o319. doi: 10.1107/S1600536810054012.
In the title molecular salt, 2C(6)H(14)N(+)·C(14)H(8)O(4)S(2) (2-), the complete dianion is generated by crystallographic twofold symmetry and a twisted conformation is found [the C-S-S-C torsion angle is 87.13 (2)° and the dihedral angle between the rings is 83.4 (2)°]. In the crystal, inter-molecular N-H⋯O hydrogen bonds link the cations and anions.
2. Cyclo-hexyl-ammonium nitrate
Abdulaziz A Bagabas, Mohamed F A Aboud, Ahsan M Shemsi, Emad S Addurihem, Zeid A Al-Othman, C S Chidan Kumar, Hoong-Kun Fun Acta Crystallogr Sect E Struct Rep Online. 2014 Feb 5;70(Pt 3):o253-4. doi: 10.1107/S1600536814002244. eCollection 2014 Mar 1.
In the title salt, C6H14N(+)·NO3 (-), the cyclo-hexyl ring adopts a chair conformation. The ammonium group occupies an equatorial position and the crystal struture is stabilized by inter-molecular N-H⋯O hydrogen-bonding inter-actions, resulting in a three-dimensional network.
3. Synthesis of α-D-Ribose 1-Phosphate and 2-Deoxy-α-D-Ribose 1-Phosphate Via Enzymatic Phosphorolysis of 7-Methylguanosine and 7-Methyldeoxyguanosine
Irina V Varizhuk, Vladimir E Oslovsky, Pavel N Solyev, Mikhail S Drenichev, Sergey N Mikhailov Curr Protoc. 2022 Jan;2(1):e347. doi: 10.1002/cpz1.347.
A simple and efficient method for the preparation of α-D-ribose 1-phosphate and 2-deoxy-α-D-ribose 1-phosphate, key intermediates in nucleoside metabolism and important starting compounds for the enzymatic synthesis of various modified nucleosides, has been proposed. It consists in near-irreversible enzymatic phosphorolysis of readily prepared hydroiodide salts of 7-methylguanosine and 7-methyl-2'-deoxyguanosine, respectively, in the presence of purine nucleoside phosphorylase. α-D-Ribose 1-phosphate and 2-deoxy-α-D-ribose 1-phosphate are obtained in near quantitative yields (by HPLC analysis) and 74%-94% yields after their isolation and purification. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Preparation of α-D-ribose 1-phosphate barium salt (4a) Alternate Protocol 1: Preparation of 2-deoxy-α-D-ribose 1-phosphate barium salt (4b) Basic Protocol 2: Preparation of α-D-ribose 1-phosphate bis(cyclohexylammonium) salt (5a) Alternate Protocol 2: Preparation of 2-deoxy-α-D-ribose 1-phosphate bis(cyclohexylammonium) salt (5b).
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