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((3aR,6S,6aS)-6-(6-amino-9H-purin-9-yl)-5-fluoro-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol is a complex organic molecule that features a purine base (6-amino-9H-purin-9-yl) attached to a cyclopenta[d][1,3]dioxol ring structure. This ring is further bonded to a methanol group, and the compound also includes a fluorine atom and two methyl groups. These structural elements contribute to the compound's unique properties, which may have potential pharmaceutical applications, particularly in drug discovery and development. The presence of the purine base, a key component of many biologically active molecules, makes ((3aR,6S,6aS)-6-(6-aMino-9H-purin-9-yl)-5-fluoro-2,2-diMethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)Methanol an interesting subject for research and potential applications in medicine and biotechnology.

805245-45-8

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805245-45-8 Usage

Uses

Used in Pharmaceutical Industry:
((3aR,6S,6aS)-6-(6-amino-9H-purin-9-yl)-5-fluoro-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol is used as a potential candidate for drug discovery and development due to its complex structure and the presence of a purine base. The purine base is a key component of many biologically active molecules, which makes ((3aR,6S,6aS)-6-(6-aMino-9H-purin-9-yl)-5-fluoro-2,2-diMethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)Methanol a promising candidate for further research and development in the pharmaceutical industry.
Used in Biotechnology Industry:
In the biotechnology industry, ((3aR,6S,6aS)-6-(6-amino-9H-purin-9-yl)-5-fluoro-2,2-dimethyl-6,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)methanol may be utilized for the development of novel therapeutic agents or as a component in the design of new biotechnological processes. Its unique structure and properties could be harnessed to create innovative solutions in various biotechnological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 805245-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,5,2,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 805245-45:
(8*8)+(7*0)+(6*5)+(5*2)+(4*4)+(3*5)+(2*4)+(1*5)=148
148 % 10 = 8
So 805245-45-8 is a valid CAS Registry Number.

805245-45-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ((3aS,4S,6aR)-4-(6-amino-9H-purin-9-yl)-5-fluoro-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-6-yl)methanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:805245-45-8 SDS

805245-45-8Downstream Products

805245-45-8Relevant academic research and scientific papers

Design, synthesis and anticancer activity of fluorocyclopentenyl-purines and – pyrimidines

Yoon, Ji-seong,Jarhad, Dnyandev B.,Kim, Gyudong,Nayak, Akshata,Zhao, Long Xuan,Yu, Jinha,Kim, Hong-Rae,Lee, Ji Yun,Mulamoottil, Varughese A.,Chandra, Girish,Byun, Woong Sub,Lee, Sang Kook,Kim, Yong-Chul,Jeong, Lak Shin

, p. 406 - 417 (2018/06/26)

Based on the potent anticancer activity of 6′-fluorocyclopentenyl-cytosine 2b in phase IIa clinical trials for the treatment of gemcitabine-resistant pancreatic cancer, we carried out a systematic structure-activity relationship study of 6′-fluorocyclopen

Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase

Moon, Hyung Ryong,Lee, Kang Man,Lee, Hyun Joo,Lee, Sang Kook,Park, Seung Bin,Chun, Moon Woo,Jeong, Lak Shin

, p. 707 - 708 (2007/10/03)

Four 5′-substituted fluoro-neplanocin A analogues 1a-d were designed and synthesized, and the inhibitory activity against SAH was in the following order: NH2 > SH > F, N3, indicating a hydrogen bonding donor is essential for inhibito

Synthesis of 5′-substituted fluoro-neplanocin A analogues: Importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase

Moon, Hyung Ryong,Lee, Hyun Joo,Kim, Kyung Ran,Lee, Kang Man,Lee, Sang Kook,Kim, Hea Ok,Chun, Moon Woo,Jeong, Lak Shin

, p. 5641 - 5644 (2007/10/03)

Four 5′-substituted fluoro-neplanocin A analogues 1a-d were designed and synthesized to study structure-activity relationship against SAH. The inhibitory activity against SAH was in the following order: NH2 > SH > F, N3, indicating a

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