N-BOC-SERINOL, 97 CAS 125414-41-7

Introduction:Basic information about N-BOC-SERINOL, 97 CAS 125414-41-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

N-BOC-SERINOL, 97 Basic information

Product Name:N-BOC-SERINOL, 97
Synonyms:CarbaMic acid,N-[2-hydroxy-1-(hydroxyMethyl)ethyl]-, 1,1-diMethylethyl ester;N-Boc-serinol 97%;t-Butyl 1,3-dihydroxypropan-2-ylcarbamate;2-(Boc-amino)-1,3-propanediol;tert-Butyl (1,3-dihydroxypropan-2-yl);tert-butyl N-[2-hydroxy-1-(hydroxymethyl)ethyl]carbamate;N-BOC-SERINOL, 97;Carbamic acid, [2-hydroxy-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester
CAS:125414-41-7
MF:C8H17NO4
MW:191.22
EINECS:
Product Categories:N-BOC
Mol File:125414-41-7.mol

N-BOC-SERINOL, 97 Chemical Properties

Melting point 85-89 °C
Boiling point 363.0±32.0 °C(Predicted)
density 1.136±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Solid
pka11.60±0.46(Predicted)
color White to off-white
InChIInChI=1S/C8H17NO4/c1-8(2,3)13-7(12)9-6(4-10)5-11/h6,10-11H,4-5H2,1-3H3,(H,9,12)
InChIKeyJHBKBRLRYPYBLP-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)NC(CO)CO

Safety Information

Hazard Codes Xi
Risk Statements 36
Safety Statements 26
WGK Germany 3
HS Code 2924190090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2

N-BOC-SERINOL, 97 Usage And Synthesis

DescriptionT-Butyl 1,3-dihydroxypropan-2-ylcarbamate is a branched PEG derivative with biotin and two hydroxyl moieties. The hydroxyl groups enable further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.
UsesN-Boc-serinol is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1].
Synthesis

24424-99-5

534-03-2

125414-41-7

The general procedure for the synthesis of N-BOC-serinol from di-tert-butyl dicarbonate and serinol was as follows: di-tert-butyl dicarbonate (24.0 g, 0.1 mol) was added to an ethanol (100 mL) solution of serinol (1.00 g, 0.1 mol). The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the reaction solution was concentrated to dryness under vacuum to afford N-BOC-serinol (21.0 g, yield: 100%) as a white solid.

IC 50Alkyl/ether
References[1] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562 DOI:10.1016/j.ebiom.2018.09.005

N-BOC-SERINOL, 97 Preparation Products And Raw materials

Raw materialsCarbonic acid, bis(1,1-dimethylethyl) ester-->Di-tert-butyl dicarbonate-->2-Amino-1,3-propanediol
Preparation Products2-((tert-Butoxycarbonyl)amino)propane-1,3-diyl dimethanesulfonate-->Carbamic acid, [2-amino-1-(aminomethyl)ethyl]-, 1,1-dimethylethyl ester (9CI)
N-BOC-O-Benzyl-L-serine CAS 23680-31-1
N-Bromosuccinimide CAS 128-08-5
Recommended......
TOP