1-(Diphenylmethyl)piperazine is an intermediate during drug synthesis. It has been reported to be formed during the oxidative metabolism of cinnarizine (CZ) [1-(diphenylmethyl)-4-(3-phenyl-2-propenyl)-piperazine] in rat liver microsomes.[1] It reacts with quinone in acetonitrile, followed by oxidation with an alkaline potassium ferricyanide, to afford 4-amino-3,6-di(tert-butyl)-o-benzoquinones.Application1-(Diphenylmethyl)piperazine [N-(Diphenylmethyl)piperazine] may be used for the synthesis of 2-nitro-3,4,4-trichloro-1-(propylthio)-1-[4-(diphenylmethyl)piperazin-1-yl]-1,3-butadiene and 2-nitro-3,4,4-trichloro-1-(octadecylthio)-1-[4-(diphenylmethyl)piperazin-1-yl]-1,3-butadiene.
Specifications and Purity: ≥98%(GC)
MDL Number: MFCD00038379
Molecular Formula: C17H20N2
Molecular Weight: 252.36
PubChem CID: 70048
Isomeric SMILES: C1CN(CCN1)C(C2=CC=CC=C2)C3=CC=CC=C3
Beilstein Registry Number: 222773
Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/B134038-SCI_c23d51d9111b8c1aad2d28291e8c0914.pdf
- UPC:
- 51171915
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- B134038-5g
- CAS:
- 841-77-0
- Product Size:
- 5g
- Hazard Statement Codes:
- H302
- Precautionary Statement Codes:
- P501:P403+P233:P405:P362+P364:P305+P351+P338:P304+P340:P302+P352:P301+P312:P330:P280:P271:P270:P264:P261
akash.verma@cenmed.com
(732) 447-1115





