CAS No.2162-74-5,Bis(2,6-diisopropylphenyl)carbodiimide Suppliers

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Basic Information

Molecular Structure:
CAS No.:	2162-74-5
Name:	Bis(2,6-diisopropylphenyl)carbodiimide
Article Data:	14
Cas Database

Formula:	C₂₅H₃₄N₂
Molecular Weight:	362.558
Synonyms:	Carbodiimide,bis(2,6-diisopropylphenyl)- (7CI,8CI);Additin RC 8500;Bis(2,6-diisopropylphenyl)carbodiimide;Bis(o,o'-diisopropylphenyl)carbodiimide;Carbo D;EN 160;N,N'-(2,2',6,6'-Tetraisopropyldiphenyl)carbodiimide;N,N'-Bis(2,6-diisopropylphenyl)carbodiimide;Raschig 7000;Stabaxol 1;StabaxolI;Stabaxol I-LF;Stabaxol P 1;Stabilizer 7000;Stabilizer 7000F;
EINECS:	218-487-5
Density:	0.953 g/cm³
Melting Point:	51 °C
Boiling Point:	477.699 °C at 760 mmHg
Flash Point:	235.604 °C
Solubility:	50μg/L at 20℃
Appearance:	White to off-white crystalline powder
Risk Codes:	36/37/38
Safety:	26-36/37/39
PSA:	24.72000
LogP:	8.31730

Synthetic route

: 25348-97-4
N,N'-bis(2,6-diisopropylphenyl)thiourea

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
With bis(trichloromethyl) carbonate; sodium hydrogencarbonate In ethyl acetate at 20℃; for 0.25h;	95%
With dmap; iodine In tetrahydrofuran at 0 - 20℃; Reagent/catalyst;	90%
With magnesium sulfate; mercury(II) oxide In toluene for 12h; Reflux;	87%

: 201230-82-2
carbon monoxide

: C21H44CoNP3

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
In toluene at 20℃; under 760.051 Torr; for 0.166667h; Mechanism;	86%

: 28178-42-9
2,6-diisopropylphenyl isocyanate

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
With 3,4-dimethyl-1-phenyl-3-phospholene 1-oxide In xylene for 12h; Heating;	78%
at 150℃;
With methylphospholene oxide at 160 - 170℃;

: 7564-51-4
2,5-dihydro-3-methyl-1-phenyl-1H-phosphole 1-oxide

: 28178-42-9
2,6-diisopropylphenyl isocyanate

A bis(2,6diisopropylphenyl)carbodimide: bis(2,6diisopropylphenyl)carbodimide

B: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
	A 1.43 g (79%) B n/a

...Expand

: 24544-04-5
2,6-diisopropylbenzenamine

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: triethylamine / water 2: tetrachloromethane; triphenylphosphine; triethylamine / dichloromethane View Scheme
Multi-step reaction with 2 steps 1: triethylamine / water / Inert atmosphere; Schlenk technique 2: triethylamine; triphenylphosphine / tetrachloromethane; dichloromethane / Inert atmosphere; Schlenk technique View Scheme

: [Cu((methylcarbodiimide)-2,6-diisopropylphenylimidazolium)2]+[BPh4-]

A: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

B: C10H16CuN4(1+)*C24H20B(1-)

Conditions

Conditions	Yield
In chlorobenzene at 90℃; for 2h; Inert atmosphere; Schlenk technique;

: 136551-45-6
2,6-diisopropyl-1-azidobenzene

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diethyl ether / 0.5 h / 20 °C 2: toluene / 0.17 h / 20 °C / 760.05 Torr View Scheme

: 109-99-9
tetrahydrofuran

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

: 591-51-5
phenyllithium

: 1512828-35-1
[PhC(NC6H4iPr2-2,6)2]Li(THF)

Conditions

Conditions	Yield
In dibutyl ether at 20℃; for 2h;	100%

...Expand

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

: 75-24-1
trimethylaluminum

: (MeC(N-(2,6-diisopropylphenyl))2)AlMe2

Conditions

Conditions	Yield
In hexane at 20℃; Schlenk technique; Inert atmosphere;	99%
In hexane N2-atmosphere; addn. of soln. of AlMe3 (slight excess) to soln. of carbodiimide, stirring at room temp. for 18 h; evapn.; NMR spectroscopy;	74%

: 2162-74-5
N,N'-bis(2,6-diisopropylphenyl)carbodiimide

: 536-74-3
phenylacetylene

: (E)-N,N'-bis(2,6-diisopropylphenyl)-3-phenylpropiolamidine

Conditions

Conditions	Yield
Stage #1: phenylacetylene With (tri(3,5-dimethylpyrazolyl)borate)CpGd(CH2Ph)(THF) In toluene for 0.5h; Inert atmosphere; Glovebox; Schlenk technique; Stage #2: N,N'-bis(2,6-diisopropylphenyl)carbodiimide In toluene at 110℃; for 22h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Time; Concentration; Inert atmosphere; Glovebox; Schlenk technique;	99%

Raw Materials

Downstream Products

Total:114 Page 1 of 3 1 2 3 Next>>

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Chemistry

Product Name:Bis-(2,6-diisopropylphenyl)carbodiimide(2162-74-5)
CAS No:2162-74-5
Molecular Formula : C₂₅H₃₄N₂Molecular Formula:362.55
CBNumber : CB1347186
Formula Weight : 362.55
MP : 51 °C
Synonyms of Bis-(2,6-diisopropylphenyl)carbodiimide(2162-74-5):BIS(2,6-DIISOPROPYLPHENYL)CARBODIIMIDE;(2,6-diisopropylphenyl)carbodiimide;2,2’,6,6’-Tetraisopropyldiphenylcarbodiimide;bis(2,6-diisopropylphenyl)-carbodiimid;carbod;n,n’-methanetetraylbis(2,6-bis(1-methylethyl)-benzenamin;n,n’-methanetetraylbis(2,6-bis(1-methylethyl)benzenamine);n,n’-methanetetraylbis[2,6-bis(1-methylethyl)-benzenamin
Molecular Structure of Bis-(2,6-diisopropylphenyl)carbodiimide(2162-74-5):

Toxicity Data With Reference

1.	orl-rat LD50:200 mg/kg	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .
2.	ihl-rat LCLo:100 mg/m3/6H	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .
3.	ipr-rat LD50:200 mg/kg	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .
4.	ihl-mus LCLo:1 g/m3/1H	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .
5.	ihl-rbt LCLo:100 mg/m3/6H	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .
6.	ihl-gpg LCLo:100 mg/m3/6H	NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0545280 .

Safety Profile

A poison by ingestion, intraperitoneal, and inhalation. When Bis-(2,6-diisopropylphenyl)carbodiimide was heated to decomposition, it emits toxic vapors of NO_x.
Risk Statements 36/37/38
Safety Statements 26-36/37/39
RTECS CY0887250