121653-99-4

• 

• Basic information

  1. Product Name: 2,3-Butadien-1-ol, 4-(6-amino-9H-purin-9-yl)-, (R)-
  2. Synonyms:
  3. CAS NO:121653-99-4
  4. Molecular Formula: C9H9N5O
  5. Molecular Weight:
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 121653-99-4.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 2,3-Butadien-1-ol, 4-(6-amino-9H-purin-9-yl)-, (R)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2,3-Butadien-1-ol, 4-(6-amino-9H-purin-9-yl)-, (R)-(121653-99-4)
  11. EPA Substance Registry System: 2,3-Butadien-1-ol, 4-(6-amino-9H-purin-9-yl)-, (R)-(121653-99-4)

• 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: 121653-99-4(Hazardous Substances Data)

• Suppliers
• Usage
• Upstream product
• Downstream Products
• Article

121653-99-4 Suppliers

Recommended suppliersmore

• Product
• FOB Price
• Min.Order
• Supply Ability
• Supplier
• Contact Supplier

121653-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121653-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121653-99:
(8*1)+(7*2)+(6*1)+(5*6)+(4*5)+(3*3)+(2*9)+(1*9)=114
114 % 10 = 4
So 121653-99-4 is a valid CAS Registry Number.

121653-99-4Upstream product

• 66224-66-6 adenine 
• 114978-79-9 4-(6-Amino-purin-9-yl)-but-2-yn-1-ol 
• 114987-15-4 N⁹-(4-Chloro-2-butyn-1-yl)adenine 
• 114987-18-7 adenallene 

121653-99-4Downstream Products

121653-99-4Relevant articles and documents

Nucleic Acid Derived Allenols: Unusual Analogues of Nucleosides with Antiretroviral Activity

Phadtare, Shashikant,Zemlicka, Jiri

, p. 5925 - 5931 (2007/10/02)

Racemic 1,2-butadien-4-ols substituted with a nucleic acid base were prepared by a base-catalyzed isomerization of the corresponding 2-butynols.With basic heterocycles such as adenine, cytosine, 5-methylcytosine, or N-guanine, the respective allenes were obtained without difficulty, but with guanine, side reactions were observed.Reaction of 2-butynols in stronger base (1 M NaOH) gave cyclized products-oxacyclopentenes 8a-c. (+/-)-Adenallene (3a) and (+/-)-cytallene (3c) are strong inhibitors of replication of human immunodeficiency virus(HIV) in vitro. (+/-)-Adenallene (3a) and butyne 6a are substrates for adenosine deaminase.Racemic 3a was deaminated quantitatively to (+/-)-hypoxallene (3h), indicating a low stereoselectivity as contrasted with the natural substrate-adenosine.When the deamination was stopped ad ca. 50percent conversion, (-)-adenallene (3a) and (+)-hypoxallene (3h) were obtained.Antiretroviral and adenosine deaminase substrate activities are discussed in terms of the similarity of several steric and stereoelectronic features of allenic derivatives of nucleic bases with those of the corresponding nucleosides or 2',3'-dideoxyribonuclesides.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 121653-99-4 2,3-Butadien-1-ol, 4-(6-amino-9H-purin-9-yl)-, (R)-

Send

Send

Metric Ton KG G Pound L ML

Send

Send