missing translation for 'onlineSavingsMsg'
Learn More

Phenyl chlorothionoformate, 98+%, Thermo Scientific Chemicals

Catalog Number p-7043452
Click to view available options
Quantità:
1 g
5 g
25 g
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
1005-56-7
C7H5ClOS
172.63
MFCD00004920
KOSYAAIZOGNATQ-UHFFFAOYSA-N
o-phenyl carbonochloridothioate, phenyl chlorothionoformate, o-phenyl chlorothioformate, phenyl chlorothioformate, phenyl thioxochloroformate, phenyl chlorothionocarbonate, phenoxythiocarbonyl chloride, chlorothioformic acid phenyl ester, o-phenyl chlorothionoformate, o-phenyl chlorothiocarbonate
70498
ClC(=S)OC1=CC=CC=C1
Les retours ne sont pas autorisés pour ce produit. Consulta la politica di reso
To receive the discount customers must purchase three of the same product at list price in a single order to receive 33% discount. There is no limit to the multiples of 3 that customers can buy. Use promo code ”21615” to get your promotional price
1005-56-7
C7H5ClOS
172.63
MFCD00004920
KOSYAAIZOGNATQ-UHFFFAOYSA-N
o-phenyl carbonochloridothioate, phenyl chlorothionoformate, o-phenyl chlorothioformate, phenyl chlorothioformate, phenyl thioxochloroformate, phenyl chlorothionocarbonate, phenoxythiocarbonyl chloride, chlorothioformic acid phenyl ester, o-phenyl chlorothionoformate, o-phenyl chlorothiocarbonate
70498
ClC(=S)OC1=CC=CC=C1

Phenyl chlorothionoformate has been used in stereo directed synthesis of optically active, (-)-mintlactone, synthesis of peptide α-thioesters having a variety of C-terminal amino acids, synthesis of scyllo-inositol derivatives, thionocarbonylation of unprotected thymine nucleosides, preparation of phenoxythiocarbonyl esters of protected ribonucleosides. It is also used as a reagent in the thionocarbonylation of unprotected thymine nucleosides. It forms phenoxythiocarbonyl esters of protected ribonucleosides which can be reduced by tributyltin hydride to deoxyribonucleosides.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Phenyl chlorothionoformate has been used in stereo directed synthesis of optically active, (-)-mintlactone, synthesis of peptide α-thioesters having a variety of C-terminal amino acids, synthesis of scyllo-inositol derivatives, thionocarbonylation of unprotected thymine nucleosides, preparation of phenoxythiocarbonyl esters of protected ribonucleosides. It is also used as a reagent in the thionocarbonylation of unprotected thymine nucleosides. It forms phenoxythiocarbonyl esters of protected ribonucleosides which can be reduced by tributyltin hydride to deoxyribonucleosides.

Solubility
Soluble in water.

Notes
Moisture, Heat Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.
TRUSTED_SUSTAINABILITY
Materiale o nome chimico Phenyl chlorothionoformate
Densità 1.248
Punti di ebollizione 81°C to 83°C (6 mmHg)
Punto d'infiammabilità 81°C (177°F)
Odore Acrid
Indice di rifrazione 1.5804
Quantità 1 g
Numero UN UN3265
Beilstein 774830
Sensibilità Moisture sensitive
Informazioni di solubilità Soluble in water.
IUPAC Name phenyl chloromethanethioate
Peso formulazione 172.63
Percent Purity ≥98%
Vedi altri risultati Mostra meno risultati

RUO – Research Use Only

missing translation for 'provideContentCorrection'

missing translation for 'productTitle'