137022-81-2

Basic information

• Product Name: (3-Amino-4,5-dimethoxy-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester
• Synonyms: (3-Amino-4,5-dimethoxy-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester
• CAS NO: 137022-81-2
• Molecular Weight: 312.441
• Mol File: 137022-81-2.mol

Chemical Properties

• CAS DataBase Reference: (3-Amino-4,5-dimethoxy-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Amino-4,5-dimethoxy-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester(137022-81-2)
• EPA Substance Registry System: (3-Amino-4,5-dimethoxy-phenyl)-carbamic acid 2-trimethylsilanyl-ethyl ester(137022-81-2)

Safety Data

• Hazardous Substances Data: 137022-81-2(Hazardous Substances Data)

Upstream product

• 137022-84-5 1-benzyloxycarbonylamino-2,3-dimethoxy-5-(2-trimethylsilylethoxy)carbonylaminobenzene 
• 155989-60-9 3-Benzyloxycarbonylamino-4,5-dimethoxy-benzoic acid 
• 137022-83-4 3-benzyloxycarbonylamino-4,5-dimethoxybenzaldehyde 
• 22027-96-9 5-nitroveratral 
• 2916-68-9 2-(Trimethylsilyl)ethanol 

Downstream Products

• 137022-86-7 1-Benzyl-7-methoxy-3,4-dihydro-1H-pyrrolo[4,3,2-de]quinolin-8-one 
• 137043-27-7 1-benzyl-6,7-dimethoxy-1,3,4,5-tetrahydropyrrolo<4,3,2-de>quinolin-4-one 
• 137022-91-4 7-<<2-(3,5-dibromo-4-hydroxyphenyl)ethyl>amino>-1,3,4,8-tetrahydropyrrolo<4,3,2-de>quinolin-8-one 
• 137022-85-6 1-benzylamino-2,3-dimethoxy-5-(2-trimethylsilylethoxy)carbonylaminobenzene 
• 105372-81-4 discorhabdin C 
• 137022-87-8 1-benzyl-7-<<2-(3,5-dibromo-4-hydroxyphenyl)ethyl>amino>-1,3,4,8-tetrahydropyrrolo<4,3,2-de>quinolin-8-one 
• 137022-89-0 5-benzyl-11,13-dibromo-2,3,5,7,8,9-hexahydro-12-hydroxy-6H-pyrrolo<4',3',2':4,5>quino<8,7-a><3>benzazepin-6-one 
• 137022-88-9 N-Benzyl discorhabdin C 
• 137043-26-6 1-benzyl-6,7-dimethoxy-3-etoxycarbonylmethyl-4-(2-trimethylsilylethoxy)carbonylaminoindole 
• 1027537-14-9 (4-Amino-6,7-dimethoxy-1H-indol-3-yl)-acetic acid 
• 137022-82-3 (4-Amino-1-benzyl-6,7-dimethoxy-1H-indol-3-yl)-acetic acid ethyl ester 

Relevant articles and documents

Synthetic studies on tetrahydropyrroloquinoline-containing natural products: Syntheses of discorhabdin C, batzelline C and isobatzelline C

Discorhabdin C (1), batzelline C (2) and isobatzelline C (3), metabolites of marine sources sharing a tetrahydropyrroloquinoline core, have been successfully synthesized, and cytotoxicities of several synthetic intermediates were evaluated.

Synthetic studies on novel sulfur-containing alkaloids, prianosins and discorhabdins: Total synthesis of discorhabdin C

The first total synthesis of discorhabdin C, related to the cytotoxic sulfur-containing alkaloids prianosins and discorhabdins is described. The crucial phenolic oxidation of the appropriate phenol carrying no protective group was achieved by electrochemi