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Merck
CN

337005

1,3-二氯-1,1,3,3-四异丙基二硅氧烷

97%

别名:

TIPDSiCl2

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关于此项目

线性分子式:
[(CH3)2CH]2Si(Cl)OSi(Cl)[CH(CH3)2]2
化学文摘社编号:
分子量:
315.43
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1934216
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产品名称

1,3-二氯-1,1,3,3-四异丙基二硅氧烷, 97%

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

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pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

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

存储类别

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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)
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

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