105748-60-5

• 

• Basic information

  1. Product Name: 1-METHOXYBRASSININ
  2. Synonyms: 1-METHOXYBRASSININ;[(1-Methoxy-1H-indole-3-yl)methyl]dithiocarbamic acid methyl ester;1-Methoxy-1H-indole-3-ylmethyldithiocarbamic acid methyl ester;1-Methoxy-3-(methylthiocarbonothioylaminomethyl)-1H-indole;Methoxybrassinin;N-[(1-Methoxy-1H-indol-3-yl)methyl]dithiocarbamic acid methyl ester
  3. CAS NO:105748-60-5
  4. Molecular Formula: C₁₂H₁₄N₂OS₂
  5. Molecular Weight: 266.38236
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 105748-60-5.mol
  9. Article Data: 7

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 422.9°Cat760mmHg
  3. Flash Point: 209.6°C
  4. Appearance: /
  5. Density: 1.25g/cm³
  6. Vapor Pressure: 2.33E-07mmHg at 25°C
  7. Refractive Index: 1.634
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 1-METHOXYBRASSININ(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1-METHOXYBRASSININ(105748-60-5)
  12. EPA Substance Registry System: 1-METHOXYBRASSININ(105748-60-5)

• 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: 105748-60-5(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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105748-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105748-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,7,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105748-60:
(8*1)+(7*0)+(6*5)+(5*7)+(4*4)+(3*8)+(2*6)+(1*0)=125
125 % 10 = 5
So 105748-60-5 is a valid CAS Registry Number.

InChI:InChI=1/C12H14N2OS2/c1-15-14-8-9(7-13-12(16)17-2)10-5-3-4-6-11(10)14/h3-6,8H,7H2,1-2H3,(H,13,16)

105748-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	methyl N-[(1-methoxyindol-3-yl)methyl]carbamodithioate

1.2 Other means of identification

Product number	-
Other names	Methoxybrassinin

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:105748-60-5 SDS

105748-60-5Upstream product

• 74-93-1 methylthiol 
• 126769-93-5 1-methoxyindolyl-3-methyl isothiocyanate 
• 74-88-4 methyl iodide 
• 5187-84-8 1-methoxy-3-indolylmethyl glucosinolate 
• 69111-61-1 1-methoxyindole-3-carboxaldehyde oxime 
• 132169-26-7 (1-methoxyindol-3-yl)methylamine 
• 487-89-8 Indole-3-carboxaldehyde 
• 5457-28-3 3-cyano-1H-indole 
• 81794-61-8 N'-acetyl-3-indolylmethanamine 
• 22259-53-6 3-aminomethylindole 
• 141524-66-5 N-(2,3-Dihydro-1H-indol-3-ylmethyl)-acetamide 
• 180910-52-5 N-(1-Hydroxy-1H-indol-3-ylmethyl)-acetamide 
• 141524-67-6 N-(1-Methoxy-1H-indol-3-ylmethyl)-acetamide 
• 141524-68-7 2,2,2-Trifluoro-N-(1H-indol-3-ylmethyl)-acetamide 

105748-60-5Downstream Products

• 960207-26-5 (2S,3S)-1-methoxyspirobrassinol (1R,2S,5R)-menthyl ether 
• 960207-08-3 (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether 
• 1430400-16-0 1-methoxy-2-phenylbrassinin 
• 1430400-18-2 1-methoxy-2-(4-chlorophenyl)brassinin 

105748-60-5Relevant articles and documents

2-(Substituted phenyl)amino analogs of 1-methoxyspirobrassinol methyl ether: Synthesis and anticancer activity

Kutschy, Peter,Salayova, Aneta,Curillova, Zuzana,Kozar, Tibor,Mezencev, Roman,Mojzis, Jan,Pilatova, Martina,Balentova, Eva,Pazdera, Pavel,Sabol, Marian,Zburova, Michaela

, p. 3698 - 3712 (2009)

New analogs of indole phytoalexin 1-methoxyspirobrassinol methyl ether have been designed by replacement of its 2-methoxy group with 2-(substituted phenyl)amino group. Synthesized by spirocyclization methodology, trans- and cis-diastereoisomers of target

Sinalbins A and B, phytoalexins from Sinapis alba: Elicitation, isolation, and synthesis

Pedras, M.Soledade C,Zaharia, Irina L

, p. 213 - 216 (2000)

The chemical structure and synthesis of sinalbin A is described. This cruciferous phytoalexin is produced by white mustard (Sinapis alba) after treatment with biotic and abiotic elicitors. In addition, a related metabolite, named sinalbin B, is present in extracts from elicited plants, but not in those from non-elicited controls. Sinalbin B, which was also synthesized appears to be both a phytoalexin and a biosynthetic precursor of sinalbin A. (C) 2000 Elsevier Science Ltd.

A SIMPLE SYNTHESIS OF A PHYTOALEXIN, METHOXYBRASSININ

Somei, Masanori,Kobayashi, Kensuke,Shimizu, Kazuhisa,Kawasaki, Toshiya

, p. 77 - 80 (2007/10/02)

A simple and an alternative multi-gram scale synthetic method methoxybrassinin is developed starting from indole-3-carboxaldehyde.

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