1200461-84-2

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 1200461-82-0 9-[β-D-3’,5’-O-bis-(tert-butyldimethylsilyl)-2’-deoxyribofuranosyl]-2-(tert-butyldimethylsilyl)amino-6-chloro-7-methoxycarbonyl-7-deazapurine 
• 1200461-80-8 9-[β-D-3’,5’-O-bis-(tert-butyldimethylsilyl)-2’-deoxyribofuranosyl]-2-(tert-butyldimethylsilyl)amino-6-chloro-7-iodo-7-deazapurine 
• 1200461-78-4 C₁₁H₁₂ClIN₄O₃ 

Downstream Products

• 1200461-88-6 2-amino-6-chloro-9-[β-D-2‘-deoxy-ribofuranosyl]-7-(2-nitrobenzyloxy)methyl-7-deazapurine 
• 1200461-90-0 7-(2-nitrobenzyloxy)methyl-7-deaza-2’-deoxyguanosine 
• 1200463-33-7 7-(2-nitrobenzyloxy)methyl-7-deaza-2‘-deoxyguanosine-5‘-triphosphate 
• 1372854-56-2 2-amino-6-chloro-9-[β-D-2’-deoxyribofuranosyl]-7-[(S)-1-(2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deazapurine 
• 1372854-61-9 2-amino-6-methoxy-9-[β-D-2'-deoxyribofuranosyl]-7-[(S)-1-(2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deazapurine 
• 1372854-58-4 7-[(S)-1-(2-nitrophenyl)-2,2-dimethyl-propyloxy]methyl-7-deaza-2'-deoxyguanosine 
• 1372854-60-8 7-[(S)-1-(2-nitrophenyl)-2,2-dimethylpropyloxy]methyl-7-deaza-2‘-deoxyguanosine-5’-triphosphate 

Relevant academic research and scientific papers

5-METHOXY. 3'-OH UNBLOCKED, FAST PHOTOCLEAVABLE TERMINATING NUCLEOTIDES AND METHODS FOR NUCLEIC ACID SEQUENCING

The present invention relates generally to 3'-OH unblocked nucleotides and nucleosides labeled and unlabeled with 5-methoxy-substituted nitrobenzyl-based photocleavable terminating groups for use in methods and systems related to DNA and RNA sequencing an

Stereochemistry of benzylic carbon substitution coupled with ring modification of 2-nitrobenzyl groups as key determinants for fast-cleaving reversible terminators

A complete set of 2-nitrobenzyl-modified reversible terminators have been developed, which upon exposure to UV light generate natural hydroxymethyl nucleotides (see scheme). The combination of a stereospecific (S)-tert-butyl group (R) at the benzylic carb