24123-12-4

Basic information

• Product Name: 1-(benzyloxycarbonyl)-3-methylimidazolium chloride
• Synonyms: 1-(benzyloxycarbonyl)-3-methylimidazolium chloride
• CAS NO: 24123-12-4
• Molecular Weight: 252.7
• Mol File: 24123-12-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(benzyloxycarbonyl)-3-methylimidazolium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxycarbonyl)-3-methylimidazolium chloride(24123-12-4)
• EPA Substance Registry System: 1-(benzyloxycarbonyl)-3-methylimidazolium chloride(24123-12-4)

Safety Data

• Hazardous Substances Data: 24123-12-4(Hazardous Substances Data)

Upstream product

• 616-47-7 1-methyl-1H-imidazole 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 1947-00-8 6-(benzyloxycarbonylamino)hexanoic acid 
• 115538-88-0 Benzoic acid (2R,3S,5R)-5-[6-benzoylamino-8-(10-benzyloxycarbonylamino-decylamino)-purin-9-yl]-2-[(2-cyano-ethoxy)-hydroxy-phosphoryloxymethyl]-tetrahydro-furan-3-yl ester 
• 115244-16-1 C₄₉H₅₃N₇O₈ 
• 115260-06-5 6-N-benzoyl-8-<10-benzyloxycarbonyl aminodecyl>-3'-O-benzoyl-2'-deoxyadenosine 
• 115244-10-5 6-N-benzoyl-8<10-benzyloxycarbonyl aminodecyl>-amino-2'-deoxyadenosine 
• 115244-14-9 Morpholin-4-yl-phosphonic acid mono-{(2R,3S,5R)-5-[6-amino-8-(10-benzyloxycarbonylamino-decylamino)-purin-9-yl]-3-hydroxy-tetrahydro-furan-2-ylmethyl} ester 
• 115244-11-6 {10-[6-Amino-9-((2R,4S,5R)-4-hydroxy-5-phosphonooxymethyl-tetrahydro-furan-2-yl)-9H-purin-8-ylamino]-decyl}-carbamic acid benzyl ester 
• 1054645-97-4 Phenoxy-acetic acid (2R,3R,4R,5R)-5-[((S)-2-benzyloxycarbonylamino-4-methyl-pentyloxy)-hydroxy-phosphoryloxymethyl]-4-(2-phenoxy-acetoxy)-2-[6-(2-phenoxy-acetylamino)-purin-9-yl]-tetrahydro-furan-3-yl ester 
• 6216-67-7 Adenosin-5'-phosphorsaeure-(N-benzyloxycarbonyl-L-leucinolat) 
• 6216-61-1 (S)-(-)-N-(benzyloxycarbonyl)leucinol 
• 115244-09-2 8-<10-(benzyloxycarbonyl)aminodecyl>-amino-2'-deoxyadenosine 

Relevant articles and documents

POLYIMIDE PRECURSOR COMPOSITION AND PREPARATION METHOD AND USE THEREOF

The present invention provides a polyimide precursor composition comprising a polyimide precursor and a thermal base generator having the structure of formula (1): wherein R1, R2, R3, R4, R5 and are as defined in the specification. The present invention also provides a polyimide prepared from the aforementioned precursor composition, and a preparation method thereof.

Synthesis of peptidinol adenylates

Peptidinol adenylates were assembled by condensing the carboxyl group of N-blocked peptides with the alkylamino group of leucinol 5' adenosine phosphodiester. The latter was prepared as protected precursor from adenosine and leucinol by phosphite chemistry. The title compounds, which mimic aminoacyl adenylates, are designed to penetrate microorganisms via peptide permeases and to interfere with genetic translation.