137090-44-9

• 

• Basic information

  1. Product Name: CHEMBRDG-BB 4013762
  2. Synonyms: CHEMBRDG-BB 4013762;4-(CHLOROMETHYL)-5-METHYL-2-(4-METHYLPHENYL)-1,3-OXAZOLE;4-(CHLOROMETHYL)-5-METHYL-2-P-TOLYLOXAZOLE;4-(chloromethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole(SALTDATA: FREE);Oxazole, 4-(chloromethyl)-5-methyl-2-(4-methylphenyl)-
  3. CAS NO:137090-44-9
  4. Molecular Formula: C₁₂H₁₂ClNO
  5. Molecular Weight: 221.68
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 137090-44-9.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 350.6°C at 760 mmHg
  3. Flash Point: 165.8°C
  4. Appearance: /
  5. Density: 1.16g/cm³
  6. Vapor Pressure: 8.8E-05mmHg at 25°C
  7. Refractive Index: 1.547
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 0.15±0.26(Predicted)
  11. CAS DataBase Reference: CHEMBRDG-BB 4013762(CAS DataBase Reference)
  12. NIST Chemistry Reference: CHEMBRDG-BB 4013762(137090-44-9)
  13. EPA Substance Registry System: CHEMBRDG-BB 4013762(137090-44-9)

• Safety Data

  1. Hazard Codes: Xn
  2. Statements: 22
  3. Safety Statements: N/A
  4. WGK Germany: 3
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 137090-44-9(Hazardous Substances Data)

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137090-44-9 Suppliers

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• Oxazole, 4-(chloromethyl)-5-methyl-2-(4-methylphenyl)-

  Cas No: 137090-44-9

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• 5

• Hangzhou J&H Chemical Co., Ltd.
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• 4-(Chloromethyl)-5-methyl-2-p-tolyloxazole

  Cas No: 137090-44-9

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• Hangzhou Dingyan Chem Co., Ltd
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• 4-(chloromethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole(SALTDATA: FREE)

  Cas No: 137090-44-9

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• 4-(Chloromethyl)-5-methyl-2-p-tolyloxazole

  Cas No: 137090-44-9

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• Hangzhou Fandachem Co.,Ltd
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• 4-(chloromethyl)-5-methyl-2-p-tolyloxazole

  Cas No: 137090-44-9

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• SAGECHEM LIMITED
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• 4-(Chloromethyl)-5-methyl-2-p-tolyloxazole

  Cas No: 137090-44-9

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• Hangzhou Haiqiang Chemical Co.,Ltd.
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• FT-0748241

  Cas No: 137090-44-9

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• Finetech Industry Limited
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• 4-(Chloromethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole

  Cas No: 137090-44-9

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• Debye Scientific
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137090-44-9 Usage

General Description

CHEMBRDG-BB 4013762 is a chemical compound with the molecular formula C9H14N2O3S. It is an amide derivative and belongs to the class of heterocyclic compounds. CHEMBRDG-BB 4013762 is used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceutical products. It has potential pharmacological activities and is utilized in drug discovery and development processes. Its unique chemical properties make it a valuable ingredient in the production of therapeutic agents. The compound is also studied for its biological activities and interactions, making it an important compound in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 137090-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137090-44:
(8*1)+(7*3)+(6*7)+(5*0)+(4*9)+(3*0)+(2*4)+(1*4)=119
119 % 10 = 9
So 137090-44-9 is a valid CAS Registry Number.

InChI:InChI=1/C12H12ClNO/c1-8-3-5-10(6-4-8)12-14-11(7-13)9(2)15-12/h3-6H,7H2,1-2H3

137090-44-9 Well-known Company Product Price

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• Aldrich

• (CBR00539)  4-(Chloromethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole  Aldrich^CPR

• 137090-44-9

• CBR00539-1G

• 1,159.47CNY

• Detail

137090-44-9SDS

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	4-(chloromethyl)-5-methyl-2-(4-methylphenyl)-1,3-oxazole

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:137090-44-9 SDS

137090-44-9Upstream product

• 104-87-0 4-methyl-benzaldehyde 

137090-44-9Downstream Products

• 946419-17-6 (5-methyl-2-p-tolyl-oxazol-4-ylmethyl)-triphenyl-phosphonium chloride 
• 1119451-22-7 1-((5-methyl-2-(p-tolyl)oxazol-4-yl)methyl)piperidine-4-carboxylic acid 
• 1065332-86-6 (R)-2-(4-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)benzyl)thiazolidine-4-carboxylic acid 
• 1065332-88-8 (4-(5-methyl-2-p-tolyloxazol-4-ylmethoxy)phenyl)acetaldehyde 
• 1065333-95-0 (R)-1-(3-((5-methyl-2-phenyloxazol-4-yl)methoxy)benzyl)pyrrolidine-2-carboxylic acid 
• 866641-18-1 2-[4-[[carboxymethyl-(5-methyl-2-p-tolyloxazol-4-ylmethyl)amino]methyl]-2,6-dimethylphenoxy]-2-methylpropanoic acid ethyl ester 
• 1268705-38-9 (E)-ethyl 2-(4-(cyclohexyl(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)methyl)-2-methylphenoxy)acetate 
• 1268705-37-8 (E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)butyl)phenoxy)acetate 
• 1268705-36-7 (E)-ethyl 2-(4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate 
• 1268705-35-6 (E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate 
• 1268705-34-5 (E)-ethyl 2-(4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)ethyl)phenoxy)acetate 
• 1268705-33-4 (E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-(p-tolyl)oxazol-4-yl)methoxy)imino)ethyl)phenoxy)acetate 

137090-44-9Relevant articles and documents

1,3-Oxazole-isoniazid hybrids: Synthesis, antitubercular activity, and their docking studies

Katariya, Kanubhai D.,Shah, Shailesh R.

, (2020/01/25)

A series of novel N′-([2-aryl-5-methyl-1,3-oxazole-4-yl]methylene)isonicotino/nicotino hydrazides 10a-l were prepared by the condensation reaction of 2-aryl-5-methyl-1,3-oxazole-4-carbaldehydes 8a-f with the corresponding isonicotino/nicotino hydrazides 9

SUBSTITUTED ACID DERIVATIVES USEFUL AS ANTIDIABETIC AND ANTIOBESITY AGENTS AND METHOD

-

Page/Page column 29, (2010/11/29)

Compounds are provided which have the structure of Formula (I): wherein R is hydrogen or C1-C4 alkyl; and each of R1 and R2 is independently hydrogen, C1-C4 alkyl, halo or C1-Cs

METHOD FOR THE PRODUCTION OF OXAZOLES BY CONDENSING AROMATIC ALDEHYDES WITH A-KETOXIMES TO N-OXIDES AND THEN REACTING THE SAME WITH ACTIVATED ACID DERIVATIVES

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Page/Page column 18, (2008/06/13)

Disclosed is a method for producing oxazoles of formula IV by condensing aromatic aldehydes with a-ketoximes to N-oxides and then reacting the same with activated acid derivatives. The invention relates to a method for producing oxazoles by condensing ald

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