84592-35-8 | Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	2 weeks	$182.00	$128.00
1g	95%	2 weeks	$347.00	$243.00
5g	95%	2 weeks	$1,007.00	$705.00

Description

• Catalog Number: AB47732
• Chemical Name: Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate
• CAS Number: 84592-35-8
• Molecular Formula: C14H28N2O4S
• Molecular Weight: 320.4481
• MDL Number: MFCD00077676
• SMILES: O=C(OC(C)(C)C)NN(C(=O)OC(C)(C)C)SC(C)(C)C

Upstream Synthesis Route

Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and functional group compatibility. This compound serves as a valuable building block for the preparation of various organic molecules, particularly in the field of medicinal chemistry and material science.In chemical synthesis, Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate can be employed as a masked source of hydrazine functionality. Upon activation, the tert-butylthio group can be selectively removed under mild conditions, revealing the highly reactive hydrazine moiety. This strategic manipulation allows for controlled and efficient incorporation of hydrazine into target molecules, enabling the synthesis of diverse compounds such as hydrazones, hydrazides, and hydrazines.Furthermore, the tert-butyl groups on the hydrazinedicarboxylate scaffold provide steric protection, preventing unwanted side reactions and enhancing the overall selectivity of the synthetic transformations. This feature makes Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate an attractive precursor for the functionalization of complex molecules, offering chemists a powerful tool for the construction of intricate chemical structures.Overall, the application of Di-tert-butyl 1-(tert-butylthio)-1,2-hydrazinedicarboxylate in chemical synthesis showcases its utility as a versatile and efficient reagent for the selective introduction of hydrazine functionality, facilitating the synthesis of novel organic compounds with diverse applications.