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(R)-tert-Butylsulfinamide

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(R)-tert-Butylsulfinamide

Chiral · CAT No. CS-O-10921 · CAS No. 196929-78-9
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For Research & Analytical Purposes. Not for Personal use.
Clearsynth product packaging

Packaging & Handling

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Documentation Available
Detailed specifications, certificates, and supporting documents are available upon request.
Storage: Refer MSDS for complete information.
Hazard: Refer MSDS for complete information.

(R)-tert-Butylsulfinamide Product Information

(R)-tert-Butylsulfinamide is listed under Chiral and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-O-10921.

Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight and product enquiry details.

Technical Data

Product Name
(R)-tert-Butylsulfinamide
CAS No.
196929-78-9
CAT No.
CS-O-10921
HSN Code
38229010
Country of Origin
Can be shipped from India, Canada and USA
Molecular Formula
C4H11NOS
Molecular Weight
121.20
Category
Storage Condition
Refer MSDS for complete information.
Hazard Compound
Refer MSDS for complete information.

Description

Regulatory Description
(R)-tert-Butylsulfinamide is supplied with detailed characterization data compliant with regulatory guideline. (R)-tert-Butylsulfinamide can be used for analytical method development, method validation (AMV), Quality Control (QC), ANDA-related analytical work, and commercial pharmaceutical research applications.
Overview
"(R)-tert-Butylsulfinamide is a chiral ligand used in pharmaceutical compositions. (R)-tert-Butylsulfinamide can be readily transformed into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asy"
Synonyms
(R)-tert-Butylsulfinamide
Application Notes
"(R)-tert-Butylsulfinamide is a chiral ligand used in pharmaceutical compositions. (R)-tert-Butylsulfinamide can be readily transformed into P,N-sulfinyl imine ligands through condensation with aldehydes and ketones, which can undergo iridium-catalyzed asy"
References

Product Applications & Regulatory Search Terms

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