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AKOS 2004

Diethyl 2,5-dibromoadipate

CAS: 869-10-3

Molecular Formula: C10H16Br2O4

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AKOS 2004 - Names and Identifiers

Name Diethyl 2,5-dibromoadipate
Synonyms AKOS 2004
Diethyl a'd-dibromoadipate
Diethylmeso-dibromoadipate
Diethyl 2,5-dibromoadipate
DIETHYL A,A'-DIBROMOADIPATE
2,5-dibromo-diethyl adipate
DIETHYL 2,5-DIBROMOHEXANEDIOATE
Diethyl 2,5-dibromohexanedioate
DIETHYL-ALPHA,ALPHA'-DIBROMOADIPATE
diethyl (2R,5S)-2,5-dibromohexanedioate
2,5-Dibromohexanedioic acid diethyl ester
hexanedioic acid, 2,5-dibromo-, diethyl ester
ethyl (2S,5S)-2,5-dibromo-5-propanoyloxy-pentanoate
CAS 869-10-3
EINECS 200-059-4
InChI InChI=1/C10H16Br2O4/c1-3-9(13)16-8(12)6-5-7(11)10(14)15-4-2/h7-8H,3-6H2,1-2H3/t7-,8+/m0/s1
InChIKey UBCNJHBDCUBIPB-UHFFFAOYSA-N

AKOS 2004 - Physico-chemical Properties

Molecular FormulaC10H16Br2O4
Molar Mass360.04
Density1.7082 (rough estimate)
Melting Point65-67 °C (lit.)
Boling Point134°C/0.5mmHg(lit.)
Flash Point170.4°C
Solubility DCM
Vapor Presure2.59E-05mmHg at 25°C
AppearanceCrystallization
ColorBrown
Storage Conditionunder inert gas (nitrogen or Argon) at 2–8 °C
SensitiveLight Sensitive
Refractive Index1.5010 (estimate)
MDLMFCD00075379
Physical and Chemical PropertiesWhite crystals. Melting point 9.5 °c. Soluble in alcohol, ether, acetone, insoluble in water.

AKOS 2004 - Risk and Safety

Hazard SymbolsC - Corrosive
Corrosive
Risk CodesR34 - Causes burns
R36/37 - Irritating to eyes and respiratory system.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S27 - Take off immediately all contaminated clothing.
S28 - After contact with skin, wash immediately with plenty of soap-suds.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDsUN 3261 8/PG 2
WGK Germany3
HS Code29171900
Hazard Class8
Packing GroupIII

AKOS 2004 - Reference Information

Use diethyl Glutaric acid (dibromoadipic acid) is an intermediate for the synthesis of polyenoic acid, polyenoic acid is a metabolite found in the urine of workers exposed to benzene for a long time.
production method adipic acid and thionyl chloride are reacted to generate adipyl chloride, which is then reacted with bromine to obtain dibromoadipyl chloride, diethyl 2, 5-dibromoadipate was finally obtained by esterification with ethanol.
Last Update:2024-04-09 20:52:54
AKOS 2004
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