185963-33-1

Basic information

• Product Name: 3,5-BIS[(BOC-AMINO)METHYL]-BENZOIC ACID
• Synonyms: 3,5-BIS[(BOC-AMINO)METHYL]-BENZOIC ACID
• CAS NO: 185963-33-1
• Molecular Formula: C₁₉H₂₈N₂O₆
• Molecular Weight: 380.438
• Mol File: 185963-33-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-BIS[(BOC-AMINO)METHYL]-BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-BIS[(BOC-AMINO)METHYL]-BENZOIC ACID(185963-33-1)
• EPA Substance Registry System: 3,5-BIS[(BOC-AMINO)METHYL]-BENZOIC ACID(185963-33-1)

Safety Data

• Hazardous Substances Data: 185963-33-1(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 185963-32-0 3,5-bis(aminomethyl)benzoic acid dihydrochloride 
• 29333-41-3 methyl 3,5-bis(bromomethyl)benzoate 
• 25081-39-4 methyl 3,5-dimethylbenzoate 
• 499-06-9 3,5-dimethylbenzoic acid 
• 185963-31-9 methyl 3,5-bis((N-formylformamido)methyl)benzoate 

Downstream Products

• 185963-34-2 3,5-Bis-(tert-butoxycarbonylamino-methyl)-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 185963-35-3 11-[3,5-Bis-(tert-butoxycarbonylamino-methyl)-benzoylamino]-undecanoic acid 

Relevant articles and documents

GLUCOSE SENSITIVE INSULIN DERIVATIVES

The present invention relates to novel insulin derivatives and their use in the treatment or prevention of medical conditions relating to diabetes. The insulin derivatives are glucose sensitive and display glucose-sensitive albumin binding. The invention

164. Hydrolytical cleavage of TAR-RNA, the trans-Activation responsive region of HIV-1, by a bis(guanidinium) catalyst attached to arginine

Guanidinium compounds imitating the bis(arginine) structural motif of staphylococcal nuclease (e.g. 3) are known to be powerful catalysts for phosphoryl transfer reactions in dipolar aprotic solvents. Compound 3 also accelerates the hydrolysis of RNA (Hs