(S,S)-(-)-1,4-Dimethoxy-2,3-butanediol

(S,S)-(-)-1,4-Dimethoxy-2,3-butanediol

Chemicals & Biochemicals

Article No

CDX-D0434-M250

Size

250 mg

Shipping Information

RT

Article No

CDX-D0434-M250

Size

250 mg

Shipping Information

RT

Specifications

CAS No 50622-10-1
MW 150.17
Article No CDX-D0434-M250
Country Availability SE, FI, DK, NO, IS, EE, LV, LT
Description (S,S)-(-)-1,4-Dimethoxy-2,3-butanediol
Supplier Adipogen Life Sciences
Format Powder
Notes Building block for synthesis. For chiral auxiliary modification of LAH. Condensation of ester enolates and chiral imines to beta-lactams. Auxiliary, reactions of its acetal. Determination of the enantiomeric purity of ketones by acetal formation and 13C-NMR.|Chemical. CAS: 50622-10-1. Formula: C6H14O4. MW: 150.17. Synthetic Building block for synthesis. For chiral auxiliary modification of LAH. Condensation of ester enolates and chiral imines to beta-lactams. Auxiliary, reactions of its acetal. Determination of the enantiomeric purity of ketones by acetal formation and 13C-NMR.
Molecular Formula C6H14O4
Alias Names 1,4-Di-O-methyl-L-threitol
Product Type Chemicals & Biochemicals
Purity >99%
Shipping Information RT
Size 250 mg
Solubility Soluble in chloroform.
Stability Stable for at least 2 years after receipt when stored at +4°C.
Storage 4°C
Technical Specifications Chemical. CAS: 50622-10-1. Formula: C6H14O4. MW: 150.17. Synthetic Building block for synthesis. For chiral auxiliary modification of LAH. Condensation of ester enolates and chiral imines to beta-lactams. Auxiliary, reactions of its acetal. Determination of the enantiomeric purity of ketones by acetal formation and 13C-NMR.
Product Page Updated 2024-02-01T08:25:01.492Z

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