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408433

Sigma-Aldrich

Boc-His-OH

99%

Synonym(s):

Nα-(tert-Butoxycarbonyl)-L-histidine, Nα-Boc-L-histidine

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About This Item

Empirical Formula (Hill Notation):
C11H17N3O4
CAS Number:
17791-52-5
Molecular Weight:
255.27
Beilstein:
755289
EC Number:
241-768-9
MDL number:
MFCD00065576
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
24865569
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

99%

optical activity

[α]20/D +26°, c = 1 in methanol

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

195 °C (dec.) (lit.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)N[C@@H](Cc1c[nH]cn1)C(O)=O

InChI

1S/C11H17N3O4/c1-11(2,3)18-10(17)14-8(9(15)16)4-7-5-12-6-13-7/h5-6,8H,4H2,1-3H3,(H,12,13)(H,14,17)(H,15,16)/t8-/m0/s1

InChI key

AYMLQYFMYHISQO-QMMMGPOBSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL8397
BCCM6455
BCCH9728
BCCC6900
BCBV2404

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Hao Zheng et al.
Pharmaceutical research, 32(6), 2038-2050 (2014-12-24)
Present study aimed at exploring advantages/disadvantages of amino acid modified trimethylated chitosan in conquering multiple gene delivery obstacles and thus providing comprehensive understandings for improved transfection efficiency. Arginine, cysteine, and histidine modified trimethyl chitosan were synthesized and employed to self-assemble
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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