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Arabinoisocytidine is a modified nucleoside found in various plant species, such as Arabidopsis thaliana and Triticum aestivum. It is a derivative of the nucleoside cytidine, with an additional arabinose sugar group attached to the ribose ring. This unique structure endows Arabinoisocytidine with potential bioactivity and makes it a promising candidate for various applications.

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  • 10212-30-3 Structure
  • Basic information

    1. Product Name: Arabinoisocytidine
    2. Synonyms: Arabinoisocytidine;2-Amino-1-beta-D-arabinofuranosyl-4(1H)-pyrimidinone;Arabinosylisocytosine;NSC 529488
    3. CAS NO:10212-30-3
    4. Molecular Formula: C9H13N3O5
    5. Molecular Weight: 243.21662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10212-30-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 545.7°Cat760mmHg
    3. Flash Point: 283.8°C
    4. Appearance: /
    5. Density: 1.89g/cm3
    6. Vapor Pressure: 3.5E-14mmHg at 25°C
    7. Refractive Index: 1.756
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Arabinoisocytidine(CAS DataBase Reference)
    11. NIST Chemistry Reference: Arabinoisocytidine(10212-30-3)
    12. EPA Substance Registry System: Arabinoisocytidine(10212-30-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10212-30-3(Hazardous Substances Data)

10212-30-3 Usage

Uses

Used in Plant Stress Response Research:
Arabinoisocytidine is used as a biomarker for plant stress response, as its levels increase in response to environmental stressors such as drought and salinity. This indicates that Arabinoisocytidine may play a role in regulating plant responses to adverse conditions, providing valuable insights into plant stress tolerance mechanisms.
Used in Pharmaceutical Development:
Arabinoisocytidine is used as a potential target for developing new plant-based pharmaceuticals or agrochemicals due to its unique structure and potential bioactivity. Its presence in plants and its ability to respond to stress suggest that it may have therapeutic properties that can be harnessed for human or agricultural applications.
Further research is needed to fully understand the biological functions and potential applications of Arabinoisocytidine in plants, which could lead to the development of novel treatments and products based on this intriguing compound.

Check Digit Verification of cas no

The CAS Registry Mumber 10212-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10212-30:
(7*1)+(6*0)+(5*2)+(4*1)+(3*2)+(2*3)+(1*0)=33
33 % 10 = 3
So 10212-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3O5/c10-9-11-5(14)1-2-12(9)8-7(16)6(15)4(3-13)17-8/h1-2,4,6-8,13,15-16H,3H2,(H2,10,11,14)

10212-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-4-one

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:10212-30-3 SDS

10212-30-3Downstream Products

10212-30-3Relevant articles and documents

Convenient synthesis of oligodeoxyribonucleotides bearing arabinofuranosyl pyrimidine derivatives and its duplex formation with complementary DNA

Ozaki, Hiroaki,Nakajima, Kiyohiro,Tatsui, Kaoru,Izumi, Chieko,Kuwahara, Masayasu,Sawai, Hiroaki

, p. 2441 - 2443 (2007/10/03)

The oligodeoxyribonucleotides bearing 2,2′-anhydro-β-D-arabinofuranosyluracil derivatives were synthesized and the modified residue was converted to β-D-arabinofuranosyluracil derivatives or β-D-arabinofuranosylisocytosine derivatives by post-synthetic modification method. The melting profiles of their ODNs with complementary DNA were studied.

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