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Key Documents

512028

Sigma-Aldrich

tert-Butyl(4-iodobutoxy)dimethylsilane

95%

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About This Item

Linear Formula:
(CH3)3CSi(CH3)2O(CH2)4I
CAS Number:
Molecular Weight:
314.28
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

contains

copper as stabilizer

refractive index

n20/D 1.48 (lit.)

bp

75 °C/0.5 mmHg (lit.)

density

1.214 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)[Si](C)(C)OCCCCI

InChI

1S/C10H23IOSi/c1-10(2,3)13(4,5)12-9-7-6-8-11/h6-9H2,1-5H3

InChI key

INGJYKISFRSCQV-UHFFFAOYSA-N

General description

tert-Butyl(4-iodobutoxy)dimethylsilane is an iodoorganosilane that can be synthesized from tert-butyl(chloro)dimethylsilane.

Application

tert-Butyl(4-iodobutoxy)dimethylsilane may be used as a reagent in the multi-step synthesis of spermine synthon and decanucleotide-spermine conjugates.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Online synthesis of diblock cationic oligonucleotides for enhanced hybridization to their complementary sequence.
Bénédicte Pons et al.
Chembiochem : a European journal of chemical biology, 7(8), 1173-1176 (2006-07-29)
Fleming I.
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 4, 266-266 (2014)

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