1217445-37-8 | (2S-(2a,5a,6b))-3,3-Dimethyl-7-oxo-6-phenylacetyl-D7-amino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 1-ethyl-piperidinium

Packsize	Purity	Availability	Price	Discounted Price
10mg		2 weeks	$835.00	$585.00
50mg		2 weeks	$1,254.00	$878.00
100mg		2 weeks	$2,073.00	$1,452.00

Description

• Catalog Number: BA58172
• Chemical Name: (2S-(2a,5a,6b))-3,3-Dimethyl-7-oxo-6-phenylacetyl-D7-amino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 1-ethyl-piperidinium
• CAS Number: 1217445-37-8
• Molecular Formula: C23H26D7N3O4S
• Molecular Weight: 454.634
• SMILES: [2H]C(c1c([2H])c([2H])c(c(c1[2H])[2H])[2H])(C(=O)N[C@@H]1C(=O)N2[C@@H]1SC([C@@H]2C(=O)O)(C)C)[2H].CCN1CCCCC1

Upstream Synthesis Route

Penicillin G-D7 N-Ethylpiperidinium Salt can be a valuable tool in chemical synthesis due to its unique properties and reactivity. This compound can serve as a catalyst or reagent in various organic reactions, particularly those involving the manipulation of functional groups or the formation of new carbon-carbon or carbon-heteroatom bonds. Its high solubility in common organic solvents makes it easily adaptable to a wide range of reaction conditions, while its stability ensures consistent performance over multiple reaction cycles. In addition, the ability of Penicillin G-D7 N-Ethylpiperidinium Salt to act as a chiral source can enable the asymmetric synthesis of complex molecules with high enantioselectivity. Whether used in traditional organic transformations or more advanced synthetic methodologies, this compound offers chemists a versatile and reliable option for achieving their synthetic goals.