15236
N,O-Bis(trimethylsilyl)carbamate
≥98.0% (T)
Synonym(s):
BSC, Trimethylsilyl N-(trimethylsilyl)carbamate
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About This Item
Linear Formula:
(CH3)3SiNHCO2Si(CH3)3
CAS Number:
Molecular Weight:
205.40
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
252-520-4
Beilstein/REAXYS Number:
2043399
MDL number:
Assay:
≥98.0% (T)
Form:
solid
InChI key
DGIJAZGPLFOQJE-UHFFFAOYSA-N
InChI
1S/C7H19NO2Si2/c1-11(2,3)8-7(9)10-12(4,5)6/h1-6H3,(H,8,9)
SMILES string
C[Si](C)(C)NC(=O)O[Si](C)(C)C
assay
≥98.0% (T)
form
solid
mp
77-83 °C
functional group
amine
Quality Level
Related Categories
Other Notes
Extremely suitable reagent for the silylation of alcohols, phenols and carboxylic acids. The only by-products are CO2 and NH3; Silyloxycarbonylation of amines; Acylisocyanates from carboxylic acid chlorides
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Filippo Pelizzaro et al.
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We aimed at assessing the impact of surveillance on long-term survival in HCC patients. From the ITA.LI.CA database, we selected 1028 cases with long (≥5 years, LS group) and 2721 controls with short-term survival (<5 years, SS group). The association
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Outcomes for patients with hematologic malignancy infected with COVID-19 have not been aggregated. The objective of this study was to perform a systematic review and meta-analysis to estimate the risk of death and other important outcomes for these patients. We
V.P. Kozyukov et al.
Current Chemical Reactions, 2, 6251-6251 (1980)
Zhur. Obshch. Khim., 50, 955-955 (1980)
V.P. Kozyukov et al.
Zhur. Obshch. Khim., 51, 239-239 (1981)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 15236 | 04053252762963 |
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