Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

365386

Sigma-Aldrich

N,N-Diisopropylcarbamoyl chloride

98%

Synonym(s):

Diisopropylcarbamic chloride, Diisopropylcarbamyl chloride, N,N-Bis(1-methylethyl)carbamic chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
[(CH3)2CH]2NCOCl
CAS Number:
19009-39-3
Molecular Weight:
163.65
Beilstein/REAXYS Number:
1754834
EC Number:
242-743-5
MDL number:
MFCD00015013
UNSPSC Code:
12352100
PubChem Substance ID:
24862514
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

bp

90-93 °C/15 mmHg (lit.)

mp

57-59 °C (lit.)

SMILES string

CC(C)N(C(C)C)C(Cl)=O

InChI

1S/C7H14ClNO/c1-5(2)9(6(3)4)7(8)10/h5-6H,1-4H3

InChI key

RSAFAYLZKCYUQW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

N,N-Diisopropylcarbamoyl chloride may be used in the preparation of:
  • 1-aryl-1-alkenyl N,N-diisopropylcarbamates
  • 1,3-diphenylallyl carbamate
  • (Z)-1,3-diphenyl-1-propenyl N,N-diisopropylcarbamate
  • (R)-1-(2-methoxy-4-methylphenyl)ethyl diisopropyl-carbamate

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The total synthesis of (-)-aplysin via a lithiation-borylation-propenylation sequence.
Fletcher CJ, et al.
Tetrahedron, 68(23), 7598-7604 (2012)
Stereoselective Intermolecular Carbolithiation of Open-Chain and Cyclic 1-Aryl-1-alkenyl N,N-Diisopropylcarbamates Coupled with Electrophilic Substitution. Observation of p-Carboxylation in a Benzyllithium Derivative.
Peters JG, et al.
Synthesis, 03, 0381-0292 (2002)
Asymmetric ?-Deprotonation and Substitution Reactions of (Z)-1, 3-Diphenyl-1-propenyl N, N-Diisopropylcarbamate.
Reuber J, et al.
European Journal of Organic Chemistry, 14, 3017-3025 (2005)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service