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337005

Sigma-Aldrich

1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane

97%

Synonym(s):

TIPDSiCl2

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About This Item

Linear Formula:
[(CH3)2CH]2Si(Cl)OSi(Cl)[CH(CH3)2]2
CAS Number:
69304-37-6
Molecular Weight:
315.43
Beilstein/REAXYS Number:
1934216
MDL number:
MFCD00009655
UNSPSC Code:
12352001
PubChem Substance ID:
24860447
NACRES:
NA.22

Quality Level

200

assay

97%

form

liquid

refractive index

n20/D 1.454 (lit.)

bp

70 °C/0.5 mmHg (lit.)

density

0.986 g/mL at 25 °C (lit.)

SMILES string

CC(C)[Si](Cl)(O[Si](Cl)(C(C)C)C(C)C)C(C)C

InChI

1S/C12H28Cl2OSi2/c1-9(2)16(13,10(3)4)15-17(14,11(5)6)12(7)8/h9-12H,1-8H3

InChI key

DDYAZDRFUVZBMM-UHFFFAOYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H290,H314

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

168.8 °F

flash_point_c

76 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCBH8117V
1451767V
1451767
1356601
1343912

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Aldrichimica Acta, 15, 11-11 (1982)
Suetying Chow et al.
Nucleosides, nucleotides & nucleic acids, 22(5-8), 583-587 (2003-10-21)
An improved strategy for the synthesis of 2'-O-methyl-guanosine (6) and 2'-MOE-guanosine (8) is reported. The regioselectivity of the alkylation was attained using a novel silicon-based protecting group, methylene-bis (diisopropyl-silylchloride) (MDPSCl2, 2). The alkylation proceeded in a chemoselective manner using NaHMDS
M Kwiatkowski et al.
Nucleic acids research, 24(23), 4632-4638 (1996-12-01)
The synthesis of oligodeoxynucleotides is marred by several problems that contribute to the formation of defective molecules. This in turn seriously limits the usefulness of such reagents in DNA diagnostics, molecular cloning, DNA structural analysis and in antisense therapy. In
The Journal of Organic Chemistry, 58, 2552-2552 (1993)
W T Markiewicz et al.
Nucleic acids symposium series, (7)(7), 115-127 (1980-01-01)
Recent results concerning the synthesis of oligoribonucleotides via the phosphotriester method, such as functionalization of ribonucleosides, new phosphorylating agents, 5'-O-sulfonylation and chromatography on Sephadex LH-20 for monitoring the removal of internucleotide phosphotriester groups, are presented. To show that efficiency of

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