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Merck

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:
35342-88-2
Molecular Weight:
205.40
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329750791
EC Number:
252-520-4
Beilstein/REAXYS Number:
2043399
MDL number:
MFCD00040476

Key Documents

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Product Name

N,O-Bis(trimethylsilyl)carbamate, ≥98.0% (T)

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

100

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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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Certificates of Analysis (COA)

Lot/Batch Number
048627/1
048627/1V

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Filippo Pelizzaro et al.
Cancers, 13(4) (2021-03-07)
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
Abi Vijenthira et al.
Blood, 136(25), 2881-2892 (2020-10-29)
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.
Zhur. Obshch. Khim., 51, 239-239 (1981)
Isabelle C Arnold et al.
The Journal of experimental medicine, 215(8), 2055-2072 (2018-07-05)
Eosinophils are predominantly known for their contribution to allergy. Here, we have examined the function and regulation of gastrointestinal eosinophils in the steady-state and during infection with Helicobacter pylori or Citrobacter rodentium We find that eosinophils are recruited to sites
V.P. Kozyukov et al.
Current Chemical Reactions, 2, 6251-6251 (1980)
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Articles

Silylation of Non-Steroidal Anti-Inflammatory Drugs

Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

Global Trade Item Number

SKUGTIN
1523604053252762963

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