100191-61-5

• 

• Basic information

  1. Product Name: Benzoyl chloride, 2-chloro-5-methoxy- (9CI)
  2. Synonyms: Benzoyl chloride, 2-chloro-5-methoxy- (9CI)
  3. CAS NO:100191-61-5
  4. Molecular Formula: C₈H₆Cl₂O₂
  5. Molecular Weight: 205.03804
  6. EINECS: N/A
  7. Product Categories: ACIDHALIDE
  8. Mol File: 100191-61-5.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Benzoyl chloride, 2-chloro-5-methoxy- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzoyl chloride, 2-chloro-5-methoxy- (9CI)(100191-61-5)
  11. EPA Substance Registry System: Benzoyl chloride, 2-chloro-5-methoxy- (9CI)(100191-61-5)

• 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: 100191-61-5(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• Benzoyl chloride,2-chloro-5-methoxy-

  Cas No: 100191-61-5

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100191-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100191-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,9 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100191-61:
(8*1)+(7*0)+(6*0)+(5*1)+(4*9)+(3*1)+(2*6)+(1*1)=65
65 % 10 = 5
So 100191-61-5 is a valid CAS Registry Number.

100191-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-chloro-5-methoxybenzoyl chloride

1.2 Other means of identification

Product number	-
Other names	2-Chlor-5-methoxy-benzoylchlorid

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:100191-61-5 SDS

100191-61-5Upstream product

• 6280-89-3 2-chloro-5-methoxybenzoic acid 

100191-61-5Downstream Products

• 1454838-66-4 2-chloro-5-methoxy-N-(pyridin-4-yl)benzamide 
• 1363333-06-5 5-amino-2-chloropyrimidine 
• 1363332-98-2 12-O-(3-(5-(2-chloro-5-methoxy-benzoylamino)-pyrimidin-2-amino)-propyl)-berbamine 
• 1383572-79-9 C₁₅H₁₄ClNO₂ 
• 910905-39-4 2-chloro-5-methoxy-N-{2-[4-(4-methyl-piperazine-1-carbonyl)-phenylamino]-pyrimidin-5-yl}-benzamide hydrochloride 
• 100062-35-9 (2-chloro-5-methoxy-phenacyl)-malonic acid 
• 103857-60-9 4-(2-chloro-5-methoxy-phenyl)-4-oxo-butyric acid 
• 98590-29-5 2-bromo-1-(2-chloro-5-methoxyphenyl)ethan-1-one 
• 99846-94-3 2-chloro-1-(2-chloro-5-methoxy-phenyl)-ethanone 
• 100119-51-5 5-(2-chloro-5-methoxy-phenyl)-5-methyl-dihydro-furan-2-one 
• 645403-23-2 N-adamantan-1-ylmethyl-(2-chloro-5-methoxy)-benzamide 

100191-61-5Relevant articles and documents

Palladium-catalyzed intramolecular C-H arylation of 2-halo-: N -Boc- N -arylbenzamides for the synthesis of N-H phenanthridinones

Hu, Quan-Fang,Gao, Tian-Tao,Shi, Yao-Jie,Lei, Qian,Yu, Luo-Ting

, p. 13879 - 13890 (2018/04/25)

A palladium catalyzed synthesis of N-H phenanthridinones was developed via C-H arylation. The protocol gives phenanthridinones regioselectively by one-pot reaction without deprotection. It exhibits broad substrate scope and affords targets in up to 95% yields. Importantly, it could be applied for the less reactive o-chlorobenzamides.

HETEROCYCLIC AMINOBERBAMINE DERIVATIVES, THE PREPARATION PROCESS AND USE THEREOF

-

Paragraph 0097; 0098, (2013/07/19)

The present invention relates to a novel berbamine derivative of formula I or a pharmaceutically acceptable salt thereof, a process for preparation of the same, a pharmaceutical composition comprising said compound and its use in manufacture of an antitumor medicament.

Anti-selective catalytic asymmetric nitroaldol reaction via a heterobimetallic heterogeneous catalyst

Nitabaru, Tatsuya,Nojiri, Akihiro,Kobayashi, Makoto,Kumagai, Naoya,Shibasaki, Masakatsu

supporting information; experimental part, p. 13860 - 13869 (2010/01/06)

Full details of an anti-selective catalytic asymmetric nitroaldol reaction promoted by a heterobimetallic catalyst comprised of Nd5O(O iPr)13, an amide-based ligand, and NaHMDS (sodium hexamethyldisilazide) are described.

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