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3,5-Dichlorobenzaldehyde

CAS No.
10203-08-4
Chemical Name:
3,5-Dichlorobenzaldehyde
Synonyms
RARECHEM AQ A2 0002;3,5-Dichlorobenzalde;Ixazomib Impurity 15;3,5-DICHLOROBENALDEHYDE;3,5-dichloro-benzaldehyd;3,5-DICHLOROBENZALDEHYDE;Benzaldehyde, 3,5-dichloro-;3,5-Dichlorobenzaldehyde>3,5-Dichlorobenzaldehyde,97%;3,5-Dichlorobenzaldehyde, Tech.
CBNumber:
CB2180799
Molecular Formula:
C7H4Cl2O
Molecular Weight:
175.01
MDL Number:
MFCD00003352
MOL File:
10203-08-4.mol
MSDS File:
SDS
Last updated:2026-06-04 16:00:12

3,5-Dichlorobenzaldehyde Properties

Melting point 63.5-65.5 °C (lit.)
Boiling point 235-240°C
Density 1.3456 (rough estimate)
refractive index 1.5756 (estimate)
Flash point 235-240°C
storage temp. Inert atmosphere,2-8°C
form powder to crystal
color White to Light yellow
Water Solubility Insoluble in water.
Sensitive Air Sensitive
BRN 2040553
InChI 1S/C7H4Cl2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChIKey CASRSOJWLARCRX-UHFFFAOYSA-N
SMILES [H]C(=O)c1cc(Cl)cc(Cl)c1
CAS DataBase Reference 10203-08-4(CAS DataBase Reference)
FDA UNII M74YU7SE79
NIST Chemistry Reference 3,5-Dichlorobenzaldehyde(10203-08-4)
EPA Substance Registry System Benzaldehyde, 3,5-dichloro- (10203-08-4)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H315-H317-H411
Precautionary statements  P261-P264-P272-P273-P280-P302+P352
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,Xi,Xn
Risk Statements  34-36/37/38-22
Safety Statements  26-36/37/39-45-22-37/39
RIDADR  UN 3261 8/PG 2
WGK Germany  3
10
Hazard Note  Corrosive
TSCA  TSCA listed
HazardClass  8
PackingGroup  III
HS Code  29130000
Storage Class 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 2
Skin Irrit. 2
Skin Sens. 1A
Limited Quantities 5.0 kg (11 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (1Kg or 1L)
NFPA 704
1
3 0

3,5-Dichlorobenzaldehyde price More Price(74)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 139408 3,5-Dichlorobenzaldehyde 97% 10203-08-4 1g $36 2023-06-20 Buy
Sigma-Aldrich 139408 3,5-Dichlorobenzaldehyde 97% 10203-08-4 5g $106 2023-06-20 Buy
TCI Chemical D2012 3,5-Dichlorobenzaldehyde >97.0%(GC) 10203-08-4 1g $24 2026-04-30 Buy
TCI Chemical D2012 3,5-Dichlorobenzaldehyde >97.0%(GC) 10203-08-4 5g $53 2026-04-30 Buy
Apolloscientific OR8438 3,5-Dichlorobenzaldehyde tech 10203-08-4 5g $28 2026-06-04 Buy
Product number Packaging Price Buy
139408 1g $36 Buy
139408 5g $106 Buy
D2012 1g $24 Buy
D2012 5g $53 Buy
OR8438 5g $28 Buy

3,5-Dichlorobenzaldehyde Chemical Properties,Uses,Production

Chemical Properties

white to slightly yellow fluffy powder

Uses

3,5-Dichlorobenzaldehyde was used as starting reagent during synthesis of β-aryl-β-amino acid enantiomers. It was used in the synthesis of dichlorophenylpyruvic acid.

Synthesis

3 5-DICHLOROTOLUENE

25186-47-4

3,5-Dichlorobenzaldehyde

10203-08-4

General procedure for the synthesis of 3,5-dichlorobenzaldehyde from 3,5-dichloro-1-methylbenzene: (1) Apparatus: a tubular reactor was installed with reference to Fig. 2, and the type of tubing was a combination of (3a + 3d) DC channels and reinforced mixed-cake rectangular flat tubes, with the diameter and volume determined according to the flow rate and reaction conditions. (2) A mixed solution was prepared by dissolving 6.06 g of cobalt acetate and 6.06 g of sodium molybdate in 200 ml of 3,5-dichlorotoluene and 200 ml of acetic acid, respectively, where n (cobalt acetate): n (3,5-dichlorotoluene) = 0.015: 1. An H2O2-acetic acid solution was prepared by dissolving 6.06 g of sodium bromide in 20% H2O2, where n (sodium bromide): n (3, 5-dichlorotoluene) = 0.015: 1. The 3,5-dichlorotoluene-acetic acid solution and H2O2-acetic acid solution were injected into a tubular reactor at a flow rate of 8.33 ml/min and 16.67 ml/min, respectively. The reactor was subjected to continuous heat exchange via a thermostatic pump maintaining n(H2O2):n(3,5-dichlorotoluene) = 2:1. A microchannel reactor shown in Fig. 2 was used, with a controlled reaction temperature of 105 °C and a residence time of 600 s. The reaction was carried out at the outlet of the tubular reactor at a flow rate of 8.33 ml/min and 8.67 ml/min, respectively. After completion of the reaction, the outlet was cooled to 0 °C and the reaction was quenched with dichloromethane. The conversion of 3,5-dichlorotoluene was analyzed by GC to be 60.8% and the yield of 3,5-dichlorobenzaldehyde was 39.2%.

References

[1] Patent: CN106588606, 2017, A. Location in patent: Paragraph 0029-0052

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3,5-Dichlorobenzaldehyde, Tech. 3,5-Dichlorobenzalde 3,5-Dichlorobenzaldehyde,97% 3,5- twochlorobenzeneforMaldehyde RARECHEM AQ A2 0002 3,5-dichloro-benzaldehyd Benzaldehyde, 3,5-dichloro- 3,5-DICHLOROBENZALDEHYDE 3,5-DICHLOROBENALDEHYDE Ixazomib Impurity 15 3,5-Dichlorobenzaldehyde> TIANFUCHEM--10203-08-4---3,5-Dichlorobenzaldehyde 10203-08-4 C7H4CI2O Cl2C6H3CHO Organic Building Blocks Aldehydes Building Blocks ALDEHYDE Carbonyl Compounds C7 Aldehydes C7 Carbonyl Compounds Aromatic Aldehydes & Derivatives (substituted) Benzaldehyde