1006-08-2

• 

• Basic information

  1. Product Name: 6-HYDROXY-7-METHYLPURINE
  2. Synonyms: 7-METHYLHYPOXANTHINE;6-HYDROXY-7-METHYLPURINE;6H-Purin-6-one, 1,7-dihydro-7-methyl- (9CI);(6S)-3-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4R,5R)-4,5-dihydroxy-2,6,6-trimethyl-1-cyclohexenyl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-6-hydroxy-2,4,4-trimethylcyclohex-2-en-1-one;7-methyl-3H-purin-6-one;7-Methyl-7H-purin-6-ol
  3. CAS NO:1006-08-2
  4. Molecular Formula: C₆H₆N₄O
  5. Molecular Weight: 150.14
  6. EINECS: N/A
  7. Product Categories: PYRIMIDINE
  8. Mol File: 1006-08-2.mol
  9. Article Data: 8

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 447.3°Cat760mmHg
  3. Flash Point: 224.3°C
  4. Appearance: /
  5. Density: 1.6g/cm³
  6. Vapor Pressure: 3.41E-08mmHg at 25°C
  7. Refractive Index: 1.772
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 6-HYDROXY-7-METHYLPURINE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 6-HYDROXY-7-METHYLPURINE(1006-08-2)
  12. EPA Substance Registry System: 6-HYDROXY-7-METHYLPURINE(1006-08-2)

• 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: 1006-08-2(Hazardous Substances Data)

• Suppliers
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• SDS
• Upstream product
• Downstream Products
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1006-08-2 Usage

General Description

6-Hydroxy-7-methylpurine is a chemical compound that falls under the class of organic compounds known as pyrrolopyrimidines. These are compounds containing a pyrrolopyrimidine, which is a purine derivative with a structure that comprises a pyrrolo[2,3-d]pyrimidine moiety. 6-Hydroxy-7-methylpurine is known to have a slightly polar nature owing to the presence of hydroxy and methyl functional groups attached to the purine base. It is considered a crucial intermediate in several biochemical processes, including DNA repair mechanisms. However, its excessive accumulation can lead to harmful effects on living organisms, necessitating well-regulated metabolic pathways for this compound. The details of its structure, properties and biological roles are a subject of ongoing research in biochemical and pharmacological contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 1006-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1006-08:
(6*1)+(5*0)+(4*0)+(3*6)+(2*0)+(1*8)=32
32 % 10 = 2
So 1006-08-2 is a valid CAS Registry Number.

InChI:InChI=1/C6H6N4O/c1-10-3-9-5-4(10)6(11)8-2-7-5/h2-3H,1H3,(H,7,8,11)

1006-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	7-methyl-3H-purin-6-one

1.2 Other means of identification

Product number	-
Other names	7-methyl-1,7-dihydro-purin-6-one

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:1006-08-2 SDS

1006-08-2Upstream product

• 110475-17-7 5-amino-3-methyl-3H-imidazole-4-carboxylic acid amide; hydrochloride 
• 77287-34-4 formamide 
• 5440-17-5 6-chloro-7-methyl-7H-purine 
• 33763-06-3 7-methylinosine 
• 4261-05-6 4-amino-1H-imidazo<4,5-c>pyridine hydrochloride 
• 3641-08-5 1,2,4-triazole-3-carboxamide 
• 87-42-3 6-chloropurine 
• 191416-90-7 4-formamido-N'-methoxy-1-methyl-1H-imidazole-5-carboxamidine 
• 52376-64-4 N⁶-methoxy-7-methyladenine 
• 115377-71-4 4-amino-1-methyl-1H-imidazole-5-carboxamide perchlorate 
• 68-12-2 N,N-dimethyl-formamide 

1006-08-2Downstream Products

1006-08-2Relevant articles and documents

Purines. LIX. An alternative synthesis of 7-alkyl-1-methyladenines by regioselective alkylation, fission, and reclosure of the adenine ring

Fujii,Saito,Suzuki,Kunugi

, p. 151 - 153 (1994)

7-Alkyl-1-methyladenines (12a,b) have been synthesized from 1-alkyl-4- aminoimidazole-5-carboxamides (5a,b) in two steps [hence from adenine (1) in six steps]. The synthesis started with dehydration (using POCl3-HCONMe2) of 5a,b, rea

OXADIAZOLE TRANSIENT RECEPTOR POTENTIAL CHANNEL INHIBITORS

-

, (2019/09/30)

The invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof wherein A, X, R1, R4 and n are as defined herein. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain.

NEW TRPA1 ANTAGONISTS

-

Page/Page column 35; 39, (2017/05/02)

The present invention relates to bicyclic heterocyclic derivatives of Forrmula (I), to the process for preparing such compounds and to their use in the treatment of a pathological condition or disease susceptible to amelioration by TRPA1 channel inhibition or antagonism.

Purines. LXXV. Dimroth rearrangement, hydrolytic deamination, and pyrimidine-ring breakdown of 7-alkylated 1-alkoxyadenines: N(1)-C(2) versus N(1)-C(6) bond fission

Itaya, Taisuke,Ito, Nobuaki,Kanai, Tae,Fujii, Tozo

, p. 832 - 841 (2007/10/03)

On treatment with boiling H2O for 5-6h, 1-alkoxy-7-alkyladenines (13) underwent hydrolytic cleavage of the N(1)-C(2) and the N(1)-C(6) bonds to produce the imidazole-5-carboxamidines (14) in 53-60% yields and the imidazole-5-carboxamides (18) i

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