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Merck
모든 사진(1)

주요 문서

21850

Sigma-Aldrich

Carbonate on polymer support

extent of labeling: ~3.5 mmol/g NaCO3- loading

동의어(들):

Amberlite™ IRA 900 NaCO3--form

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모든 사진(1)

About This Item

UNSPSC 코드:
12352128
NACRES:
NA.22

반응 적합성

reaction type: solution phase peptide synthesis
reactivity: proton reactive

라벨링 범위

~3.5 mmol/g NaCO3- loading

불순물

~20% water

기타 정보

Polymeric reagent for the conversion of alkyl halides to alcohols in an aprotic solvent [1]; Synthesis of oxazolidinones and aziridines[2]

법적 정보

Amberlite is a trademark of DuPont de Nemours, Inc.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCBS7547V
BCBK1765V
1380564V
1380564
1259519

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COA 검색

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문서 라이브러리 방문

A. Bongini et al.
Journal of the Chemical Society. Perkin Transactions 1, 1339-1339 (1986)
G. Cardillo et al.
Journal of the Chemical Society. Chemical Communications, 1309-1309 (1982)
Margaret L Eng et al.
Ecotoxicology and environmental safety, 179, 104-110 (2019-04-27)
Tetrabromobisphenol A bis(2,3-dibromopropyl) ether (TBBPA-BDBPE) is an additive flame retardant used in polyolefins and polymers. It has been detected in biota, including in avian eggs, yet little is known of its effects. We assessed the pattern of TBBPA-BDBPE concentrations in
Margaret L Eng et al.
Ecotoxicology and environmental safety, 179, 151-159 (2019-04-30)
Tetrabromobisphenol A bis(2,3-dibromopropyl ether) (TBBPA-BDBPE) and 1,2-bis(2,4,6-tribromophenoxy)ethane (BTPBE) are both brominated flame retardants (BFRs) that have been detected in birds; however, their potential biological effects are largely unknown. We assessed the effects of embryonic exposure to TBBPA-BDBPE and BTBPE in
Elena Chiurchiù et al.
Molecules (Basel, Switzerland), 24(24) (2019-12-19)
Highly functionalized furans are the key scaffolds of many pharmaceuticals and bioactive natural products. Herein, we disclose a new fruitful synthesis of polyfunctionalized furans starting from β-nitroenones and α-functionalized ketones. The protocol involves two steps promoted by solid supported species

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