160107-15-3

• 

• Basic information

  1. Product Name: N4-Benzoyl-5-methylcytidine
  2. Synonyms: N4-Benzoyl-5-methylcytidine
  3. CAS NO:160107-15-3
  4. Molecular Formula: C₁₇H₁₉N₃O₆
  5. Molecular Weight: 361.34926
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 160107-15-3.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.55±0.1 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 8.63±0.40(Predicted)
  10. CAS DataBase Reference: N4-Benzoyl-5-methylcytidine(CAS DataBase Reference)
  11. NIST Chemistry Reference: N4-Benzoyl-5-methylcytidine(160107-15-3)
  12. EPA Substance Registry System: N4-Benzoyl-5-methylcytidine(160107-15-3)

• 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: 160107-15-3(Hazardous Substances Data)

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

160107-15-3 Suppliers

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• N4-Benzoyl-5-methylcytidine

  Cas No: 160107-15-3

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• 1 Milligram

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• NewCan Biotech Limited
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• Cytidine, N-benzoyl-5-methyl-

  Cas No: 160107-15-3

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• Kono Chem Co.,Ltd
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160107-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160107-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,1,0 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 160107-15:
(8*1)+(7*6)+(6*0)+(5*1)+(4*0)+(3*7)+(2*1)+(1*5)=83
83 % 10 = 3
So 160107-15-3 is a valid CAS Registry Number.

160107-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide

1.2 Other means of identification

Product number	-
Other names	N-benzoyl-5-methylcytidine

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:160107-15-3 SDS

160107-15-3Upstream product

• 59237-68-2 2',3',5'-tri-O-benzoyl-5-methylcytidine 
• 32865-88-6 2'-O,N⁴-bis-trimethylsilyl-5-methylcytosine 
• 554-01-8 5-methylcytosin 
• 93-97-0 benzoic acid anhydride 
• 2140-61-6 5-methylcytidine 
• 98-88-4 benzoyl chloride 

160107-15-3Downstream Products

• 160107-13-1 N-{1-[(2R,3R,4R,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-tetrahydro-furan-2-yl]-5-methyl-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide 
• 160107-17-5 N-(1-{(2R,3R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3,4-dihydroxy-tetrahydro-furan-2-yl}-5-methyl-2-oxo-1,2-dihydro-pyrimidin-4-yl)-benzamide 

160107-15-3Relevant articles and documents

Oligonucleotides comprising a modified or non-natural nucleobase

-

, (2008/06/13)

One aspect of the present invention relates to a double-stranded oligonucleotide comprising at least one non-natural nucleobase. In certain embodiments, the non-natural nucleobase is difluorotolyl, nitroindolyl, nitropyrrolyl, or nitroimidazolyl. In a preferred embodiment, the non-natural nucleobase is difluorotolyl. In certain embodiments, only one of the two oligonucleotide strands comprising the double-stranded oligonucleotide contains a non-natural nucleobase. In certain embodiments, both of the oligonucleotide strands comprising the double-stranded oligonucleotide independently contain a non-natural nucleobase. In certain embodiments, the oligonucleotide strands comprise at least one modified sugar moiety. Another aspect of the present invention relates to a single-stranded oligonucleotide comprising at least one non-natural nucleobase. In a preferred embodiment, the non-natural nucleobase is difluorotolyl. In certain embodiments, the ribose sugar moiety that occurs naturally in nucleosides is replaced with a hexose sugar, polycyclic heteroalkyl ring, or cyclohexenyl group. In certain embodiments, at least one phosphate linkage in the oligonucleotide has been replaced with a phosphorothioate linkage.

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