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Di-tert-butyl N,N-diisopropylphosphoramidite

Di-tert-butyl N,N-diisopropylphosphoramidite

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Catalog Number

ACM137348868-1

Product Name

Structure

CAS

137348-86-8

Product Overview
Usage

Synonyms

MCULE-4193707779; [bis(tert-butoxy)phosphino]bis(methylethyl)amine; Di-tert-butyl N,N-diisopropylphosphoramidite, technical, ~90% (GC/31P-NMR); 137348-86-8; 6576AA; AK-88457; di-tert-butyl diisopropylphosphoramidite; YGFLCNPXEPDANQ-UHFFFAOYSA-N; MFCD00153506; RT-012302;

IUPAC Name

N-[bis[(2-methylpropan-2-yl)oxy]phosphanyl]-N-propan-2-ylpropan-2-amine;

Molecular Weight

277.389g/mol

Molecular Formula

C14H32NO2P;

Canonical SMILES

CC(C)N(C(C)C)P(OC(C)(C)C)OC(C)(C)C;

InChI

InChI=1S/C14H32NO2P/c1-11(2)15(12(3)4)18(16-13(5,6)7)17-14(8,9)10/h11-12H,1-10H3;

InChI Key

YGFLCNPXEPDANQ-UHFFFAOYSA-N;

Storage

-20°C

Complexity

217

Covalently-Bonded Unit Count

Exact Mass

277.217g/mol

H-Bond Acceptor

Heavy Atom Count

Monoisotopic Mass

277.217g/mol

Rotatable Bond Count

Topological Polar Surface Area

21.7A^2

Application

Di-tert-butyl N,N-diisopropylphosphoramidite serves as a versatile reagent primarily employed for introducing tert-butyl-protected phosphate groups, which is instrumental in the phosphorylation of biomolecules. Beyond its general application in phosphorylation, this clear, colorless liquid is also utilized in the synthesis of phosphoramidate-linked glycoconjugates. Additionally, it is a phosphinane derivative known for its potential immunomodulating activity.

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