146337-49-7

• 

• Basic information

  1. Product Name: 1-BOC-2-TRIMETHYLSILANYL-INDOLE
  2. Synonyms: N-Boc-2-trimethylsilylindole;1-BOC-2-TRIMETHYLSILANYL-INDOLE;2-trimethylsilanyl-1h-indole-1-carboxylic acid tert-butylester;N-BOC-2-TRIMETHYLSILYL INDOLE, 97+%
  3. CAS NO:146337-49-7
  4. Molecular Formula: C16H23NO2Si
  5. Molecular Weight: 289.44
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 146337-49-7.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 373.6±34.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.00±0.1 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1-BOC-2-TRIMETHYLSILANYL-INDOLE(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-BOC-2-TRIMETHYLSILANYL-INDOLE(146337-49-7)
  11. EPA Substance Registry System: 1-BOC-2-TRIMETHYLSILANYL-INDOLE(146337-49-7)

• 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: 146337-49-7(Hazardous Substances Data)

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• Henan Allgreen Chemical Co.,Ltd
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• 2-TRIMETHYLSILYL-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

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• Hangzhou Fandachem Co.,Ltd
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• 1-Boc-2-trimethylsilanyl-indole

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• Hunan Longxianng Runhui Trading Co.,Ltd
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• 1-BOC-2-TRIMETHYLSILANYL-INDOLE

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• 2-trimethylsilyl-1-indolecarboxylic acid tert-butyl ester

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• 10 Milligram

• Amadis Chemical Co., Ltd.
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• tert-Butyl 2-(trimethylsilyl)-1H-indole-1-carboxylate

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• ENAO Chemical Co, Limited
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• 1-Boc-2-trimethylsilanyl-indole

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• Nanjing Norris Pharm Technology Co., Ltd.
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• 1-BOC-2-TRIMETHYLSILANYL-INDOLE

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146337-49-7 Usage

Chemical Properties

Pale brown crystals

Check Digit Verification of cas no

The CAS Registry Mumber 146337-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 146337-49:
(8*1)+(7*4)+(6*6)+(5*3)+(4*3)+(3*7)+(2*4)+(1*9)=137
137 % 10 = 7
So 146337-49-7 is a valid CAS Registry Number.

146337-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	tert-butyl 2-trimethylsilylindole-1-carboxylate

1.2 Other means of identification

Product number	-
Other names	N-BOC-2-trimethylsilylindole

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:146337-49-7 SDS

146337-49-7Upstream product

• 25811-66-9 tert.-Butyl-trimethylsilyl-diimin 
• 75400-67-8 indole-1-carboxylic acid tert-butyl ester 
• 75-77-4 chloro-trimethyl-silane 

146337-49-7Downstream Products

146337-49-7Relevant articles and documents

Transition-Metal-Free Silylation of Unactivated C(sp2)-H Bonds withtert-Butyl-Substituted Silyldiazenes

Neil, Baptiste,Lucien, Franck,Fensterbank, Louis,Chauvier, Clément

, p. 13085 - 13090 (2021/11/01)

Aromatic organosilanes bearing C(sp2)-Si bonds have found increasing applications across the chemical science, yet are mostly produced by atom-uneconomical stoichiometric procedures. Catalytic alternatives using hydrosilanes as silicon sources

Selectivity control in gold-catalyzed hydroarylation of alkynes with indoles: Application to unsymmetrical bis(indolyl)methanes

McLean, Euan B.,Cutolo, Francesca M.,Cassidy, Orla J.,Burns, David J.,Lee, Ai-Lan

supporting information, p. 6977 - 6981 (2020/09/12)

Gold-catalyzed hydroarylation of unactivated alkynes with indoles have previously been reported to proceed with double indole addition to produce symmetrical bis(indolyl)methanes (BIMs). We demonstrate for the first time that the selectivity of the gold-c

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