1375180-02-1

Basic information

• Product Name: benzyl 3-(3,4-bis(benzyloxy)phenyl)propanoate
• Synonyms: benzyl 3-(3,4-bis(benzyloxy)phenyl)propanoate
• CAS NO: 1375180-02-1
• Molecular Weight: 452.55
• Mol File: 1375180-02-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: benzyl 3-(3,4-bis(benzyloxy)phenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3-(3,4-bis(benzyloxy)phenyl)propanoate(1375180-02-1)
• EPA Substance Registry System: benzyl 3-(3,4-bis(benzyloxy)phenyl)propanoate(1375180-02-1)

Safety Data

• Hazardous Substances Data: 1375180-02-1(Hazardous Substances Data)

Upstream product

• 1078-61-1 dihydrocaffeic acid 
• 100-44-7 benzyl chloride 
• 2107-70-2 3,4-methoxycinnamic acid 
• 100-39-0 benzyl bromide 

Downstream Products

• 1370339-83-5 3-(3,4-bis-benzyloxy-phenyl)-N-(2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-imidazol-4-ylmethyl)propionamide 
• 1370339-84-6 N-(2-n-butyl-5-chloro-3-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-imidazol-4-ylmethyl)-3-(3,4-dihydroxy-phenyl)propionamide 
• 1370339-85-7 2-[3-(3,4-bis-benzyloxy-phenyl)propyl]isoindole-1,3-dione 
• 1370339-86-8 2-n-butyl-5-chloro-3-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid[3-(3,4-bis-benzyloxyphenyl)propyl]amide 
• 1370339-87-9 2-n-butyl-5-chloro-3-[2'-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid[3-(3,4-dihydroxyphenyl)propyl]amide 
• 524004-38-4 3-[3,4-bis(benzyloxy)phenyl]propan-1-ol 
• 93559-04-7 3-(3,4-bis-benzyloxyphenyl)-propionic acid 
• 99281-96-6 3-<3,4-bis(benzyloxy)phenyl>-1-aminopropane 
• 1375180-06-5 3-(3,4-bis(benzyloxy)phenyl)propanoyl chloride 
• 1375180-08-7 C₄₃H₅₃N₃O₇ 
• 1375180-09-8 benzyl 3-(3-(3,4-bis(benzyloxy)phenyl)propanamido)propyl(4-aminobutyl)carbamate 
• 1375180-11-2 C₄₁H₄₈N₄O₅ 
• 1375180-12-3 C₆₄H₆₈N₄O₈ 
• 1375180-15-6 benzyl 4-(3-(3,4-bis(benzyloxy)phenyl)-N-(3-aminopropyl)propanamido)butyl(3-(3-(3,4-bis(benzyloxy)phenyl)propanamido)propyl)carbamate 

Relevant articles and documents

The Total Synthesis of Spermine Alkaloid Kukoamine Bimesylate

The first total synthesis of kukoamine B bimesylate was completed from 1,4-diaminobutane dihydrochloride in 12 steps with a 11.4% overall yield, and all the steps could be carried out at a kilogram scale. The cyano groups were used as the precursor of amino groups to avoid the competitive reaction delicately. The aza-Michael addition reaction, amidation and hydrogenation of the cyano group sequence was streamlined as a general approach towards the synthesis of polyamine structures.

PHOTO-CLEAVABLE PRIMER COMPOSITIONS AND METHODS OF USE

In one embodiment, the present application discloses a photo-cleavable surface binding compound of the Formula I and Formula II: wherein the variables EG, EG1, SP1, SP2, SP3, Ar and BG are as defined herein. In another embodiment, the application discloses a method for forming a coating on a surface of a substrate using the surface binding compound.

SALTS OF KUKOAMINE B, PREPARATION METHOD AND USE THEREOF

Provided are salts of kukoamine B, their preparation method and their use in preventing and treating sepsis diseases.