tert-Butyl N,N'-diisopropylcarbamimidate

Name: tert-Butyl N,N'-diisopropylcarbamimidate
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

SDS

CAS No. 71432-55-8
Cat. No. CS-W004734
Purity≥95%
MDL No.MFCD06657672

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HazMat Fee

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Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*For research and further manufacturing use only, not for direct human use.

tert-Butyl N,N'-diisopropylcarbamimidate|CS-W004734

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General Information

CAS No. 71432-55-8
Cat. No. CS-W004734
Purity ≥95%
MDL No. MFCD06657672
Storage 4°C, protect from light, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₄N₂O
Molecular Weight 200.32
Synonym(s) tert-Butyl N,N'-diisopropylimidocarbamate
SMILES CC(/N=C(OC(C)(C)C)/NC(C)C)C

Application

tert-Butyl N,N'-diisopropylcarbamimidate serves as a stable, bench-ready reagent for the efficient synthesis of imidazolium salts and guanidine derivatives. Its orthogonal reactivity enables selective functionalization in complex molecular settings, with excellent compatibility across diverse reaction conditions. The tert-butyl group facilitates straightforward deprotection under mild acidic conditions, enabling seamless integration into multi-step synthetic sequences.

Synthesis

Route1
- 100-43-6
- 96042-30-7
- 75-65-0
- ~%
- In-stock
  
  71432-55-8
References
- EP2425861 A1, ;
Route2
- 693-13-0
- 75-65-0
- ~%
- In-stock
  
  71432-55-8
References
- Journal of Organic Chemistry, , vol. 69, # 7 p. 2504 - 2508

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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SDS
COA

Computational Chemistry Data

TPSA 33.62
LogP 2.5639
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 2

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Other Classifications

Building Blocks Skeleton Fatty chain compounds

Building Blocks Functional Group Amine

Building Blocks Functional Group Ether

Chemical Synthesis Synthetic Reagents C-X(Non-Halogen) Bond Formation Alkylation (Esterification)

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