15818-31-2

• 

• Basic information

  1. Product Name: 2-(3,3-dimethylbutyl)-1H-isoindole-1,3(2H)-dione
  2. Synonyms:
  3. CAS NO:15818-31-2
  4. Molecular Formula: C₁₄H₁₇NO₂
  5. Molecular Weight: 231.2903
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15818-31-2.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 328°C at 760 mmHg
  3. Flash Point: 131.6°C
  4. Appearance: N/A
  5. Density: 1.121g/cm³
  6. Vapor Pressure: 0.000195mmHg at 25°C
  7. Refractive Index: 1.547
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-(3,3-dimethylbutyl)-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-(3,3-dimethylbutyl)-1H-isoindole-1,3(2H)-dione(15818-31-2)
  12. EPA Substance Registry System: 2-(3,3-dimethylbutyl)-1H-isoindole-1,3(2H)-dione(15818-31-2)

• 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: 15818-31-2(Hazardous Substances Data)

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• SDS
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• 1H-Isoindole-1,3(2H)-dione,2-(3,3-dimethylbutyl)-

  Cas No: 15818-31-2

• USD $ 3.0-3.0 / Kilogram

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• 15818-31-2

  Cas No: 15818-31-2

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• Henan Tianfu Chemical Co., Ltd.
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• 1H-Isoindole-1,3(2H)-dione,2-(3,3-dimethylbutyl)- cas 15818-31-2

  Cas No: 15818-31-2

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15818-31-2 Usage

General Description

2-(3,3-dimethylbutyl)-1H-isoindole-1,3(2H)-dione, also known as thalidomide, is a pharmaceutical compound with sedative, anti-inflammatory, and immunomodulatory properties. It was initially marketed as a sedative and anti-nausea medication, but was later withdrawn from the market due to its teratogenic effects, causing severe birth defects in the offspring of women who had taken the drug during pregnancy. Despite this dark history, thalidomide has found renewed interest for its potential use in treating various medical conditions, including leprosy, multiple myeloma, and certain autoimmune diseases. It is also being investigated for its anti-angiogenic and anti-tumor properties, making it a valuable compound for research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 15818-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,1 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15818-31:
(7*1)+(6*5)+(5*8)+(4*1)+(3*8)+(2*3)+(1*1)=112
112 % 10 = 2
So 15818-31-2 is a valid CAS Registry Number.

15818-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-(3,3-dimethylbutyl)isoindole-1,3-dione

1.2 Other means of identification

Product number	-
Other names	N-(3,3-Dimethylbutyl)-phthalimid

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:15818-31-2 SDS

15818-31-2Upstream product

• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 
• 677-22-5 tert-butylmagnesium chloride 
• 524-38-9 N-hydroxyphthalimide 
• 558-37-2 tert-butylethylene 
• 20213-82-5 2-(3-methyl-but-3-enyl)-2,3-dihydro-1H-isoindole-1,3-dione 
• 74-88-4 methyl iodide 

15818-31-2Downstream Products

• 15673-00-4 3,3-dimethylbutylamine 

15818-31-2Relevant articles and documents

Intermolecular Radical Mediated Anti-Markovnikov Alkene Hydroamination Using N-Hydroxyphthalimide

Lardy, Samuel W.,Schmidt, Valerie A.

, p. 12318 - 12322 (2018)

An intermolecular anti-Markovnikov hydroamination of alkenes has been developed using triethyl phosphite and N-hydroxyphthalimide. The process tolerates a wide range of alkenes, including vinyl ethers, silanes, and sulfides as well as electronically unbiased terminal and internal alkenes. The resultant N-alkylphthalimides can readily be transformed to the corresponding primary amines. Mechanistic probes indicate that the process is mediated via a phosphite promoted radical deoxygenation of N-hydroxyphthalimide to access phthalimidyl radicals.

Hydroalkylation of Olefins to Form Quaternary Carbons

Green, Samantha A.,Huffman, Tucker R.,McCourt, Ruairí O.,Van Der Puyl, Vincent,Shenvi, Ryan A.

supporting information, p. 7709 - 7714 (2019/05/22)

Metal-hydride hydrogen atom transfer (MHAT) functionalizes alkenes with predictable branched (Markovnikov) selectivity. The breadth of these transformations has been confined to π-radical traps; no sp3 electrophiles have been reported. Here we describe a Mn/Ni dual catalytic system that hydroalkylates unactivated olefins with unactivated alkyl halides, yielding aliphatic quaternary carbons.

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