Tezacaftor Enantiomer

SZ目录编号:	SZ-T060007
CAS 号	1152311-99-3
分子式	C26H27F3N2O6
分子量	520.5
投资状态	Custom Synthesis

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化学名称: (S)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1H-indol-5-yl)cyclopropane-1-carboxamide

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: FC(O1)(F)OC2=C1C=CC(C3(CC3)C(NC4=C(F)C=C(N(C[C@H](O)CO)C(C(C)(C)CO)=C5)C5=C4)=O)=C2

Tezacaftor Enantiomer is chemically (S)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1H-indol-5-yl)cyclopropane-1-carboxamide. Tezacaftor Enantiomer is supplied with detailed characterization data compliant with regulatory guideline. Tezacaftor Enantiomer can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Tezacaftor.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Tezacaftor Enantiomer

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SZ目录编号:	: SZ-T060D01
CAS 号	: 1961280-24-9
分子式	: C26H23D4F3N2O6
分子量	: 524.5
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060D02
CAS 号	: NA
分子式	: C26H21D6F3N2O6
分子量	: 526.5
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060001
CAS 号	: 1152311-62-0
分子式	: C26H27F3N2O6
分子量	: 520.5
投资状态	: In Stock

SZ目录编号:	: SZ-T060002
CAS 号	: NA
分子式	: C34H35F3N2O5
分子量	: 608.7
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060003
CAS 号	: NA
分子式	: C36H37F3N2O6
分子量	: 650.7
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060004
CAS 号	: 1152311-90-4
分子式	: C29H31F3N2O6
分子量	: 560.6
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060005
CAS 号	: 2687976-22-1
分子式	: C29H31F3N2O6
分子量	: 560.6
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060006
CAS 号	: 1432657-04-9
分子式	: C26H25F3N2O6
分子量	: 518.5
投资状态	: Custom Synthesis

SZ目录编号:	: SZ-T060007
CAS 号	: 1152311-99-3
分子式	: C26H27F3N2O6
分子量	: 520.5
投资状态	: Custom Synthesis