1723-42-8

• 

• Basic information

  1. Product Name: 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE
  2. Synonyms: 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE;4,6-dinitroisophthaloyl dichloride
  3. CAS NO:1723-42-8
  4. Molecular Formula: C₈H₂Cl₂N₂O₆
  5. Molecular Weight: 293.02
  6. EINECS: N/A
  7. Product Categories: pharmacetical
  8. Mol File: 1723-42-8.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 419.5°Cat760mmHg
  3. Flash Point: 207.5°C
  4. Appearance: /
  5. Density: 1.765g/cm³
  6. Vapor Pressure: 3.03E-07mmHg at 25°C
  7. Refractive Index: 1.64
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE(1723-42-8)
  12. EPA Substance Registry System: 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE(1723-42-8)

• 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: 1723-42-8(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 4,6-DINITRO-1,3-BENZENEDICARBONYL CHLORIDE

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• 1,3-Benzenedicarbonyldichloride, 4,6-dinitro-

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1723-42-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1723-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1723-42:
(6*1)+(5*7)+(4*2)+(3*3)+(2*4)+(1*2)=68
68 % 10 = 8
So 1723-42-8 is a valid CAS Registry Number.

InChI:InChI=1/C8H2Cl2N2O6/c9-7(13)3-1-4(8(10)14)6(12(17)18)2-5(3)11(15)16/h1-2H

1723-42-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	4,6-dinitrobenzene-1,3-dicarbonyl chloride

1.2 Other means of identification

Product number	-
Other names	Isophthaloylchloride,4,6-dinitro-(7CI,8CI)

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:1723-42-8 SDS

1723-42-8Upstream product

• 89-87-2 2,4-dimethylnitrobenzene 
• 616-72-8 4,6-dinitro-m-xylene 
• 1872-40-8 4,6-dinitrobenzene-1,3-dioic acid 

1723-42-8Downstream Products

• 57475-52-2 (4,6-dinitro-1,3-phenylene)bis(phenylmethanone) 
• 881894-62-8 dioctyl 4,6-dinitroisophthalate 
• 914783-17-8 N¹,N³-bis(4-methoxyphenyl)-4,6-dinitrobenzene-1,3-diamide 
• 914783-28-1 4,6-bis((4-methoxyphenylamino)methyl)benzene-1,3-diamine 
• 914783-23-6 4,6-diamino-N¹,N³-bis(4-methoxyphenyl)benzene-1,3-diamide 
• 1723-44-0 4,6-diacetyl-m-phenylenediamine 
• 60386-88-1 1,5-bis-benzoylamino-2,4-bis-(5-phenyl-1H-[1,2,4]triazol-3-yl)-benzene 
• 60386-89-2 3,5,9,11-tetraphenyldi(s-triazolo<4,3-c>pyrimidine)> 
• 60386-86-9 5,5'-diphenyl-1H,1'H-3,3'-(4,6-dinitro-m-phenylene)-bis-[1,2,4]triazole 
• 60378-65-6 4,6-bis-(5-phenyl-1H-[1,2,4]triazol-3-yl)-benzene-1,3-diamine 
• 881894-65-1 C₅₁H₇₇F₃N₄O₁₀ 
• 881894-73-1 C₅₁H₇₇F₃N₄O₁₄ 
• 881894-67-3 C₄₉H₇₈N₄O₉ 
• 881894-74-2 C₄₉H₇₈N₄O₁₃ 

1723-42-8Relevant articles and documents

Overcoming regioselectivity issues inherent in bis-Troeger's base preparation

Havlik, Martin,Kral, Vladimir,Dolensky, Bohumil

, p. 4867 - 4870 (2007/10/03)

(Figure Presented) Bis-Troeger's base derivatives are a new family of molecular tweezers. A major drawback to their study is a lack of commercially available precursors, ortho-nitrocarboxylic acids. A reverse synthetic strategy starting from known dinitrodicarboxylic acids, which circumvents this problem, is presented. Via this methodology regioisomeric bis-TB derivatives can be prepared selectively, using only common aromatic amines that are typically commercially available.

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