Cas 112220-31-2,(2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate

112220-31-2

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Basic information

Product Name: (2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate
Synonyms: (2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate
CAS NO:112220-31-2
Molecular Formula:
Molecular Weight: 599.557
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate(112220-31-2)
EPA Substance Registry System: (2R,3R,4R,5R)-2-((6-amino-5-nitropyrimidin-4-yl)amino)-5-((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate(112220-31-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 112220-31-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112220-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,2 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112220-31:
(8*1)+(7*1)+(6*2)+(5*2)+(4*2)+(3*0)+(2*3)+(1*1)=52
52 % 10 = 2
So 112220-31-2 is a valid CAS Registry Number.

112220-31-2Upstream product

112220-31-2Downstream Products

105798-74-1 Clitocine

112220-31-2Relevant academic research and scientific papers

Unexpected Observation of the Dimroth Rearrangement in the Ribosylation of 4-Aminopyrimidines

Baiazitov, Ramil Y.,Sydorenko, Nadiya,Ren, Hongyu,Moon, Young-Choon

, p. 5881 - 5889 (2017)

A method for the preparation of 1-(N-ribofuranosyl)-6-imino-1,6-dihydropyrimidin-4-amines 3 or 4-(N-ribofuranosyl)-6-aminopyrimidines 4 via glycosylation of 4-aminopyrimidines 2 or 5 is described. Silylated 4-aminopyrimidines 2 or 5 upon ribosylation with 1 provide products 3. When intermediates 3 contain a strongly electron-withdrawing group, such as C(4)-Cl or C(5)-NO2, they rearrange to products 4 in the presence of aqueous ammonia. A mechanism is proposed that involves a ring-opening/ring-closing (Dimroth) rearrangement.

Use of nucleoside compounds for nonsense suppression and the treatment of genetic diseases

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Page/Page column 42, (2008/06/13)

The invention encompasses nucleoside compounds, compositions comprising the compounds and methods for treating or preventing diseases associated with nonsense mutations of mRNA by administering these compounds or compositions.

Efficient synthesis of clitocine via 1,3-N (endo) to N (exo) migration: A revision to Kini's work

Choi, Hyeong-Wook,Choi, Bo Seung,Chang, Jay Hyok,Lee, Kyu Woong,Nam, Do Hyun,Kim, Young Keun,Lee, Jae Hoon,Heo, Taeho,Shin, Hyunik,Kim, No-Soo

, p. 1942 - 1944 (2007/10/03)

Efficient synthesis of clitocine has been accomplished via unprecedented 1,3-N (endo) to N (exo) migration as a key transformation. Incorporation of p-chlorobenzoyl (PCB) group as a protecting group led to the easy solidification of the intermediate of 7,

NUCLEOSIDE COMPOUNDS AND THEIR USE FOR TREATING CANCER AND DISEASES ASSOCIATED WITH SOMATIC MUTATIONS

-

Page 81, (2010/02/06)

Synthesis, Intramolecular Hydrogen Bonding, and Biochemical Studies of Clitocine, a Naturally Occurring Exocyclic Amino Nucleoside

Moss, Randall J.,Petrie, Charles R.,Meyer, Rich B.,Nord, L. Dee,Willis, Randall C.,et al.

, p. 786 - 790 (2007/10/02)

The total synthesis of clitocine (1), a nucleoside recently isolated from the mushroom Clitocybe inversa, has been accomplished.Glycosylation of 4,6-diamino-5-nitropyrimidine (4) with 1-O-acetyl-2,3,5

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