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Home > Products >  2-Chloro-3-iodopyridine

2-Chloro-3-iodopyridine CAS NO.78607-36-0

  • Min.Order: 1 Kilogram
  • Payment Terms: L/C,T/T
  • Product Details

Keywords

  • 78607-36-0

Quick Details

  • ProName: 2-Chloro-3-iodopyridine
  • CasNo: 78607-36-0
  • Molecular Formula: C5H3ClIN
  • Appearance: Slight brown to brown solid
  • Application: intermediates
  • DeliveryTime: in stock
  • PackAge: 25/KG FIBER DRUM, inner packaging: one...
  • Port: beijing
  • ProductionCapacity: 10 Metric Ton/Year
  • Purity: 98%min(HPLC)
  • Storage: Store in a cool, dry area. Keep contai...
  • Transportation: NOT RESTRICTED
  • LimitNum: 1 Kilogram

Superiority


1. Introduction of 2-Chloro-3-iodopyridine

2-Chloro-3-iodopyridine (CAS NO.78607-36-0) is a slight brown to brown solid and used as a interme

Details


1. Introduction of 2-Chloro-3-iodopyridine

2-Chloro-3-iodopyridine (CAS NO.78607-36-0) is a slight brown to brown solid and used as a intermediate. The detailed info:

Appearance:Slight brown to brown solid
CAS NO.: 78607-36-0
Assay: ≥98%(HPLC)
Formula:    C5H3ClNI
M.W.:        239.44
Feature:      Similar white to slight yellow crystal, m.p: 93-96℃, light Sensitive

We can supply its 98%min(HPLC). Our production capacity of this chemical is 10 metric ton per year. It is in stock now. We will delicery it from the beijing port. Besides, you can pay us via L/C or T/T.

2. Basic information of 2-Chloro-3-iodopyridine

1) Properties:

(1)XLogP3-AA: 2.5; (2)H-Bond Acceptor: 1; (3)Exact Mass: 238.899875; (4)MonoIsotopic Mass: 238.899875; (5)Topological Polar Surface Area: 12.9; (6)Heavy Atom Count: 8; (7)Complexity: 78.8; (8)Covalently-Bonded Unit Count: 1; (9)Feature 3D Acceptor Count: 1; (10)Feature 3D Hydrophobe Count: 1; (11)Feature 3D Ring Count: 1; (12)Effective Rotor Count: 0; (13)Conformer Sampling RMSD: 0.4; (14)CID Conformer Count: 1.

2) Descriptors of Structure

IUPAC Name: 2-chloro-3-iodopyridine
InChI: InChI=1S/C5H3ClIN/c6-5-4(7)2-1-3-8-5/h1-3H
InChIKey: OHWSWGXNZDSHLM-UHFFFAOYSA-N
Canonical SMILES: C1=CC(=C(N=C1)Cl)I
 

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