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CAS 66338-95-2

Ethyl (2Z)-4-chloro-2-(hydroxyimino)-3-oxobutanoate

Codes: Ceftazidime-046

Application context (from source-drug indications)

CystitisAvibactam Sodium/CeftazidimeCholecystitisAvibactam Sodium/CeftazidimePeritonitisAvibactam Sodium/CeftazidimeIntra-abdominal infectionAvibactam Sodium/CeftazidimeLiver abscessAvibactam Sodium/CeftazidimeSepsisAvibactam Sodium/CeftazidimeBacterial infectionCeftazidime/Tazobactam SodiumRespiratory tract infectionCeftazidime/Tazobactam SodiumUrinary tract infectionCeftazidime/Tazobactam SodiumBacterial infectionCeftazidimeGram-positive bacterial infectionCeftazidimeGram-negative bacterial infectionCeftazidimeGynaecological disorderCeftazidimeIntra-abdominal infectionCeftazidimeOsteoarthritisCeftazidime

Source drugs (routes using this intermediate)

DrugTierExpiry
Avibactam Sodium/CeftazidimeTier C — Watch / trade-
Ceftazidime/Tazobactam SodiumTier C — Watch / trade-
CeftazidimeTier C — Watch / trade-

Position in synthesis routes (up/downstream chain)

Ordered by route registration; left → right is the synthesis direction. The highlighted node is the current CAS; others link to their own profiles.

Avibactam Sodium/CeftazidimeOptimised routesteps: 1total yield: /
Ethyl (2Z)-4-chloro-2-(hydroxyimino)-3-oxobutanoate→Thiocarbamide→Ethyl (2E)-(2-amino-1,3-thiazol-4-yl)(hydroxyimino)acetate
Ceftazidime/Tazobactam SodiumOptimised routesteps: 1total yield: /
Ethyl (2Z)-4-chloro-2-(hydroxyimino)-3-oxobutanoate→Thiocarbamide→Ethyl (2E)-(2-amino-1,3-thiazol-4-yl)(hydroxyimino)acetate
CeftazidimeOptimised routesteps: 1total yield: /
Ethyl (2Z)-4-chloro-2-(hydroxyimino)-3-oxobutanoate→Thiocarbamide→Ethyl (2E)-(2-amino-1,3-thiazol-4-yl)(hydroxyimino)acetate

Intermediates available on this site

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