337005
1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane
97%
Synonym(s):
TIPDSiCl2
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
[(CH3)2CH]2Si(Cl)OSi(Cl)[CH(CH3)2]2
CAS Number:
Molecular Weight:
315.43
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1934216
Assay:
97%
Form:
liquid
InChI
1S/C12H28Cl2OSi2/c1-9(2)16(13,10(3)4)15-17(14,11(5)6)12(7)8/h9-12H,1-8H3
SMILES string
CC(C)[Si](Cl)(O[Si](Cl)(C(C)C)C(C)C)C(C)C
InChI key
DDYAZDRFUVZBMM-UHFFFAOYSA-N
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.)
Quality Level
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
168.8 °F
flash_point_c
76 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
The Journal of Organic Chemistry, 58, 2552-2552 (1993)
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service